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BENZYL 2,2,2-TRICHLOROACETIMIDATE

Product Name
BENZYL 2,2,2-TRICHLOROACETIMIDATE
CAS No.
81927-55-1
Chemical Name
BENZYL 2,2,2-TRICHLOROACETIMIDATE
Synonyms
Benzyl trichloroacetimidate;oroacetimidate;BENZYLPHOSPONIC ACID;LABOTEST-BB LT00455324;Benzyl 2,2,2-trichloroacetimide;BENZYL 2,2,2-TRICHLOROACETIMIDATE;benzyl 2,2,2-trichloroethaniMidate;Benzyl 2,2,2-trichloroethanimidoate;O-Benzyl 2,2,2-trichloroacetiMidate;TRICHLOROACETIMIDIC ACID BENZYL ESTER
CBNumber
CB8409616
Molecular Formula
C9H8Cl3NO
Formula Weight
252.52
MOL File
81927-55-1.mol
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BENZYL 2,2,2-TRICHLOROACETIMIDATE Property

Melting point:
3 °C
Boiling point:
106-114 °C0.5 mm Hg(lit.)
Density 
1.359 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.545(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Miscible with cyclohexane/dichloromethane.
form 
Liquid
pka
2.23±0.70(Predicted)
color 
Clear colorless to yellow
Sensitive 
Moisture Sensitive
BRN 
2525375
Stability:
Moisture Sensitive
InChI
InChI=1S/C9H8Cl3NO/c10-9(11,12)8(13)14-6-7-4-2-1-3-5-7/h1-5,13H,6H2
InChIKey
HUZCTWYDQIQZPM-UHFFFAOYSA-N
SMILES
C(=N)(OCC1=CC=CC=C1)C(Cl)(Cl)Cl
CAS DataBase Reference
81927-55-1(CAS DataBase Reference)
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Safety

Hazard Codes 
Xn
Risk Statements 
22-36/37/38
Safety Statements 
26
WGK Germany 
3
8-10-21
HS Code 
29252900
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
140333
Product name
Benzyl 2,2,2-trichloroacetimidate
Purity
99%
Packaging
5g
Price
$43.1
Updated
2025/07/31
Sigma-Aldrich
Product number
140333
Product name
Benzyl 2,2,2-trichloroacetimidate
Purity
99%
Packaging
25g
Price
$142
Updated
2025/07/31
TCI Chemical
Product number
B1483
Product name
Benzyl 2,2,2-Trichloroacetimidate
Purity
>97.0%(GC)
Packaging
25g
Price
$89
Updated
2025/07/31
TRC
Product number
B316075
Product name
Benzyl 2,2,2-Trichloroacetimidate
Packaging
25g
Price
$150
Updated
2021/12/16
TRC
Product number
B316075
Product name
Benzyl 2,2,2-Trichloroacetimidate
Packaging
100g
Price
$450
Updated
2021/12/16
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BENZYL 2,2,2-TRICHLOROACETIMIDATE Chemical Properties,Usage,Production

Chemical Properties

clear colorless to yellow liquid

Uses

Benzyl 2,2,2-trichloroacetimidate is used for the acid-catalyzed benzylation of hydroxy groups. It acts as reagent during the synthesis of funiculosin dimethyl ether and (S)-3-(benzyloxy)-2-methylpropanal. It can also be used for mild esterification of carboxylic acids in the presence of a catalytic amount of BF3 etherate.

Uses

Benzyl 2,2,2-trichloroacetimidate was used as reagent during the synthesis of funiculosin dimethyl ether and (S)-3-(benzyloxy)-2-methylpropanal. It was used in the acid-catalyzed benzylation of hydroxy groups.

Uses

Benzyl 2,2,2-trichloroacetimidate is used for the acid-catalyzed benzylation of hydroxy groups.

Synthesis

545-06-2

100-51-6

81927-55-1

DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) (1.24 mL, 8.31 mmol) was slowly added dropwise to a solution of dichloromethane (86 mL) containing benzyl alcohol (8.60 mL, 83.11 mmol) and trichloroacetonitrile (41.66 mL, 415.57 mmol), and the reaction mixture was cooled under ice bath conditions to 0 °C . Subsequently, the mixture was gradually warmed up to room temperature reaction. The progress of the reaction was monitored by thin layer chromatography (TLC) (petroleum ether/ethyl acetate, 95:5, V/V) until the formation of trichloroacetimide was observed. After 3 h of reaction, the solvent was removed by distillation under reduced pressure and the resulting residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, 95:5, V/V), followed by distillation at 80 °C/0.3 mbar to afford the target product 2,2,2-trichloroacetimidobenzyl ester as a colorless oil in 94% yield.TLC Rf value: 0.27 (petroleum ether/ethyl acetate. 95:5, V/V).1H NMR (400.13 MHz, CDCl3) δ (ppm): 5.26 (s, 2H, H1'); 7.24-7.36 (m, 5H, HPh); 8.31 (wide s, 1H, =NH).13C NMR (100.62 MHz, CDCl3) δ (ppm): 70.7 (Cl'); 91.3 (C2); 127.7, 128.3 and 128.5 (5C, CPh); 134.4 (C2'); 162.5 (C1).

Purification Methods

Purify the imidate by distillation to remove up to 1% of PhCH2OH as stabiliser. A solution in hexane can be stored for up to 2 months without decomposition. It is hygroscopic and has to be stored dry. [Wessel et al. J Chem Soc, Perkin Trans 1 2247 1985, Beilstein 6 IV 2265.]

References

[1] Tetrahedron Letters, 1996, vol. 37, # 9, p. 1481 - 1484
[2] Tetrahedron Letters, 2009, vol. 50, # 21, p. 2533 - 2535
[3] Bioorganic and Medicinal Chemistry Letters, 2016, vol. 26, # 2, p. 636 - 639
[4] Patent: US6348478, 2002, B1. Location in patent: Page column 32-33
[5] Journal of Organic Chemistry, 2003, vol. 68, # 19, p. 7234 - 7242

BENZYL 2,2,2-TRICHLOROACETIMIDATE Preparation Products And Raw materials

Raw materials

Preparation Products

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BENZYL 2,2,2-TRICHLOROACETIMIDATE Suppliers

Epsilon Chimie
Tel
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Fax
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Email
pierre.cornec@epsilon-chimie.com
Country
France
ProdList
687
Advantage
0
Epsilon Chimie
Tel
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Fax
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Email
pierre.cornec@epsilon-chimie.com
Country
France
ProdList
538
Advantage
61
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View Lastest Price from BENZYL 2,2,2-TRICHLOROACETIMIDATE manufacturers

Henan Aochuang Chemical Co.,Ltd.
Product
BENZYL 2,2,2-TRICHLOROACETIMIDATE 81927-55-1
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
98%
Supply Ability
1ton
Release date
2022-09-26
Shaanxi Dideu Medichem Co. Ltd
Product
BENZYL 2,2,2-TRICHLOROACETIMIDATE 81927-55-1
Price
US $0.00-0.00/KG
Min. Order
1g
Purity
99% HPLC
Supply Ability
2000tons
Release date
2019-12-30
Zhuozhou Wenxi import and Export Co., Ltd
Product
BENZYL 2,2,2-TRICHLOROACETIMIDATE 81927-55-1
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10

81927-55-1, BENZYL 2,2,2-TRICHLOROACETIMIDATERelated Search:


  • 2,2,2-TRICHLOROACETIMIDIC ACID BENZYL ESTER
  • Benzyl 2,2,2-trichloroacetimidate, 98+%
  • Ethanimidic acid, 2,2,2-trichloro-, phenylmethyl ester
  • Benzyl 2,2,2-trichloroacetimidate, GC 99%
  • BENZYLPHOSPONIC ACID
  • Benzyl 2,2,2-trichloroethanimidoate
  • Benzyl trichloroacetimidate
  • TRICHLOROACETIMIDIC ACID BENZYL ESTER
  • LABOTEST-BB LT00455324
  • BENZYL 2,2,2-TRICHLOROACETIMIDATE
  • Benzyl 2,2,2-trichloroacetimidate, 99 %
  • AcetiMidic acid, 2,2,2-trichloro-, benzyl ester (6CI)
  • O-Benzyl 2,2,2-trichloroacetiMidate
  • Benzyl 2,2,2-trichloroacetimide
  • Benzyl 2,2,2-trichloroacetimidate 99%
  • Benzyl 2,2,2-trichloroacetiMidate, 99% 25GR
  • benzyl 2,2,2-trichloroethaniMidate
  • (2,2,2-trichloro-1-phenylmethoxyethylidene)azanide
  • Benzyl 2,2,2-Trichloroacetimidate &gt
  • oroacetimidate
  • BENZYL 2,2,2-TRICHLOROACETIMIDATE ISO 9001:2015 REACH
  • Phenylmethyl 2,2,2-trichloroethanimidate
  • 81927-55-1
  • CCl3CNHOCH2C6H5
  • C9H8Cl3NO
  • Amidates/Imidates
  • Building Blocks
  • Nitrogen Compounds
  • Organic Building Blocks
  • Protection & Derivatization Reagents (for Synthesis)
  • Protection & Derivatization Reagents (for Synthesis)
  • Synthetic Organic Chemistry
  • Amidates/Imidates
  • Building Blocks
  • Chemical Synthesis
  • Nitrogen Compounds
  • Organic Building Blocks
  • Benzene series