Identification | Back Directory | [Name]
1H-Indole-1-carboxylic acid, 5-(hydroxyMethyl)-, 1,1-diMethylethyl ester | [CAS]
279255-90-2 | [Synonyms]
1-Boc-1H-indol-5-ylmethanol tert-butyl 5-(hydroxymethyl)indole-1-carboxylate 5-methylolindole-1-carboxylic acid tert-butyl ester 5-Hydroxymethyl-indole-1-carboxylic acid tert-butyl ester 5-(hydroxymethyl)-1-indolecarboxylic acid tert-butyl ester 1H-Indole-1-carboxylic acid, 5-(hydroxyMethyl)-, 1,1-diMethylethyl ester | [Molecular Formula]
C14H17NO3 | [MDL Number]
MFCD09834884 | [MOL File]
279255-90-2.mol | [Molecular Weight]
247.29 |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of tert-butyl 5-(hydroxymethyl)-1H-indole-1-carboxylate from tert-butyl 5-formyl-1H-indole-1-carboxylate: firstly, tert-butyl 5-formyl-1H-indole-1-carboxylate (12.23 mmol) was dissolved in methanol (30 mL) to obtain a solution. To this solution, sodium tetrahydroborate (0.463 g, 12.23 mmol) was slowly added at 0 °C. The reaction mixture was stirred continuously at 0 °C for 3 h, followed by stirring at room temperature overnight. After completion of the reaction, the resulting solution was diluted with water (40 mL) and extracted with ethyl acetate (3 x 30 mL). The organic layers were combined, washed sequentially with aqueous sodium carbonate and brine, dried over anhydrous sodium sulfate, and concentrated in vacuum to afford tert-butyl 5-(hydroxymethyl)-1H-indole-1-carboxylate (2.5 g, 10.11 mmol, 83% yield) as a yellow oil.LCMS analysis showed m/z = 270.3 [M + Na]+. | [References]
[1] Journal of the American Chemical Society, 2017, vol. 139, # 20, p. 6847 - 6850 [2] Patent: WO2017/216726, 2017, A1. Location in patent: Page/Page column 955 |
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Energy Chemical
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