Basic information Safety Supplier Related

tert-Butyl 2-iodoacetate

Basic information Safety Supplier Related

tert-Butyl 2-iodoacetate Basic information

Product Name:
tert-Butyl 2-iodoacetate
Synonyms:
  • IODO-ACETIC ACID TERT-BUTYL ESTER
  • tert-butyl 2-iodoacetate
  • tert-Butyl Iodoacetate
  • Acetic acid, 2-iodo-, 1,1-dimethylethyl ester
CAS:
49827-15-8
MF:
C6H11IO2
MW:
242.05
Mol File:
49827-15-8.mol
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tert-Butyl 2-iodoacetate Chemical Properties

Boiling point:
206.4±13.0 °C(Predicted)
Density 
1.614±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
Appearance
Light yellow to brown Liquid
InChI
InChI=1S/C6H11IO2/c1-6(2,3)9-5(8)4-7/h4H2,1-3H3
InChIKey
QYPDJIDQEZDFLS-UHFFFAOYSA-N
SMILES
C(OC(C)(C)C)(=O)CI
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Safety Information

RIDADR 
2810
HazardClass 
6.1
PackingGroup 
HS Code 
2915907098
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tert-Butyl 2-iodoacetate Usage And Synthesis

Uses

tert-Butyl Iodoacetate is used in the synthesis and biological evaluation of water-soluble derivative of potent V-ATPase inhibitor archazolid.

Synthesis

5292-43-3

49827-15-8

The general procedure for the synthesis of tert-butyl iodoacetate from tert-butyl bromoacetate was as follows: tert-butyl bromoacetate (6) (1.00 g, 5.13 mmol, 1.0 eq.) was slowly added dropwise to a pre-prepared solution of sodium iodide (1.15 g, 7.69 mmol, 1.5 eq.) in anhydrous acetone (30 mL). The reaction mixture was stirred continuously at room temperature for 150 min and the progress of the reaction was monitored by thin layer chromatography (TLC) [unfolding agent: petroleum ether/ethyl acetate = 2:1; Rf value of tert-butyl iodoacetate = 0.73] to confirm the complete conversion of the reaction. Subsequently, the reaction solution was filtered to remove insoluble impurities and the filtrate was concentrated by rotary evaporator. To the concentrated residue, pentane (15 mL) was added for washing and the filtrate was filtered again to remove the precipitate. Finally, the filtrate was concentrated under vacuum to afford the target product tert-butyl iodoacetate (1.01 g, 81% yield) as a light yellow oil.

References

[1] Patent: US5618808, 1997, A
[2] Angewandte Chemie - International Edition, 2010, vol. 49, # 15, p. 2738 - 2742
[3] Journal of Organic Chemistry, 2006, vol. 71, # 19, p. 7307 - 7314
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 1997, vol. 39, # 6, p. 509 - 524
[5] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 24, p. 7735 - 7738

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