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
tert-Butyl 5-(benzyloxy)-1H-indole-1-carboxylate Property
- storage temp.
- 2-8°C
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.
N-Bromosuccinimide Price
- Product number
- 127039
- Product name
- tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
- Purity
- >95%
- Packaging
- 1g
- Price
- $270
- Updated
- 2021/12/16
- Product number
- 127039
- Product name
- tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
- Purity
- >95%
- Packaging
- 5g
- Price
- $810
- Updated
- 2021/12/16
- Product number
- 61-11376
- Product name
- tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
- Purity
- 95-98%
- Packaging
- 5g
- Price
- $405
- Updated
- 2021/12/16
- Product number
- CM147574
- Product name
- tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
- Purity
- 95%
- Packaging
- 5g
- Price
- $421
- Updated
- 2021/12/16
- Product number
- CD11239379
- Product name
- tert-Butyl5-(benzyloxy)-1H-indole-1-carboxylate
- Purity
- 95+%
- Packaging
- 5g
- Price
- $446
- Updated
- 2021/12/16
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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