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tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate

Product Name
tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate
CAS No.
170147-29-2
Chemical Name
tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate
Synonyms
tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate;5-Benzyloxy-indole-1-carboxylic acid tert-butyl ester;2-methyl-2-propanyl 5-(benzyloxy)-1h-indole-1-carboxylate;5-(Benzyloxy)-1H-indole-1-carboxylic acid tert-butyl ester;1H-Indole-1-carboxylic acid, 5-(phenylmethoxy)-, 1,1-dimethylethyl ester
CBNumber
CB02723404
Molecular Formula
C20H21NO3
Formula Weight
323.39
MOL File
170147-29-2.mol
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tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate Property

storage temp. 
2-8°C
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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

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

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

Matrix Scientific
Product number
127039
Product name
tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
Purity
>95%
Packaging
1g
Price
$270
Updated
2021/12/16
Matrix Scientific
Product number
127039
Product name
tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
Purity
>95%
Packaging
5g
Price
$810
Updated
2021/12/16
Abosyn
Product number
61-11376
Product name
tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
Purity
95-98%
Packaging
5g
Price
$405
Updated
2021/12/16
Chemenu
Product number
CM147574
Product name
tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
Purity
95%
Packaging
5g
Price
$421
Updated
2021/12/16
Crysdot
Product number
CD11239379
Product name
tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
Purity
95+%
Packaging
5g
Price
$446
Updated
2021/12/16
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tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate Chemical Properties,Usage,Production

Synthesis

1215-59-4

24424-99-5

170147-29-2

Step 1: To a solution of 5-benzyloxyindole (2 g, 8.98 mmol) in dichloromethane (DCM, 20 mL) was added sequentially triethylamine (EtsN, 3.7 mL, 26.91 mmol) and 4-dimethylaminopyridine (DMAP, 328 mg, 2.68 mmol) at 0 °C, followed by the addition of di-tert-butyl dicarbonate (Boc2O. 2.9 g, 13.45 mmol). After the addition was completed, the reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the reaction mixture was diluted with dichloromethane, washed with water and saturated saline in turn, the organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and concentrated to dryness. The crude product was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate=50:1) to afford tert-butyl 5-(benzyloxy)-1H-indole-1-carboxylate (2.5 g, yield 86.08%) as a white solid. lC/MS (ESI) m/z: 268 ([M-Boc+H]+).

References

[1] Patent: WO2007/76034, 2007, A2. Location in patent: Page/Page column 126-127
[2] Organic and Biomolecular Chemistry, 2007, vol. 5, # 8, p. 1218 - 1227
[3] Chemical and Pharmaceutical Bulletin, 2000, vol. 48, # 11, p. 1689 - 1697
[4] Patent: WO2009/5998, 2009, A1. Location in patent: Page/Page column 256
[5] Chemical Communications, 2012, vol. 48, # 26, p. 3239 - 3241

tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate Preparation Products And Raw materials

Raw materials

Preparation Products

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tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate Suppliers

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170147-29-2, tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylateRelated Search:


  • tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate
  • 2-methyl-2-propanyl 5-(benzyloxy)-1h-indole-1-carboxylate
  • 1H-Indole-1-carboxylic acid, 5-(phenylmethoxy)-, 1,1-dimethylethyl ester
  • 5-Benzyloxy-indole-1-carboxylic acid tert-butyl ester
  • 5-(Benzyloxy)-1H-indole-1-carboxylic acid tert-butyl ester
  • 170147-29-2