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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521491Generated: October 30, 2026

tert-Butyl N-(2-bromoethyl)carbamate → HCID 89827882, compound

https://huagongshe.com/reaction/1521491

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl N-(2-bromoethyl)carbamateHCID 4103526—
ReactantHCID 89815985HCID 89815985—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 89827882HCID 8982788220.7%

Reaction Steps

To a solution of 2-methyl-1-(6-(methylthio)-1H-indol-2-yl)propan-1-one (600 mg, 2.57 mmol) and Bu4NBr (4.12 g, 12.85 mmol) in 9 N NaOH (10 mL, cooled) was added tert-butyl (2-bromoethyl)carbamate (2.87 g, 12.85 mmol). The reaction mixture was stirred at rt for 72 h. The mixture was diluted with water (20 mL) at 0° C., extracted with EtOAc (20 mL×3). The combined organic layers were dried over anhydrous sodium sulfate, filtered, concentrated and purified by column chromatography on silica gel eluting with PE/EtOAc 10:1 to afford tert-butyl (2-(2-isobutyryl-6-(methylthio)-1H-indol-1-yl)ethyl)carbamate (200 mg, 20.66% yield) as a colorless oil. LC-MS MS (ESI) m/z 321.1 [M-56+H]+, 277.1 [M-100+H]+. 1H NMR (CDCl3 400 MHz): δ 7.57 (d, J=8.4 Hz, 1H), 7.38 (s, 1H), 7.29 (s, 1H), 7.10 (d, J=8.4 Hz, 1H), 4.80 (brs, 1H), 4.62 (t, J=6.4 Hz, 2H), 3.58-3.42 (m, 3H), 2.58 (s, 3H), 1.38 (s, 9H), 1.24 (d, J=6.8 Hz, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073931B2
Source datasetuspto-grants-2015_07
ORD IDord-c352965b65824c5490233ee3c0b6ae7b
Source noteuspto-grants-2015_07