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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 582257Generated: October 25, 2026

Cycloheptylamine → 2-Bromo-N-(cycloheptyl)acetamide

https://huagongshe.com/reaction/582257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCycloheptylamineHCID 2899—
ReactantBromoacetyl bromideHCID 61147—
ReactantDiisopropylethylamineHCID 81531—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Bromo-N-(cycloheptyl)acetamideHCID 2225157489.7%

Reaction Steps

To a -20° C. solution of cycloheptylamine (6.37 mL, 50.0 mmol) and diisopropylethylamine (9.58 mL, 55.0 mmol) in methylene chloride (250 mL) was slowly added bromoacetyl bromide (4.78 mL, 55.0 mmol). The reaction mixture was warmed to room temperature over 20 minutes and stirred for an addition 30 minutes. The reaction mixture was diluted with water (100 mL) and stirred for an additional 30 minutes. The organic layer was separated, washed with water (3×100 mL), dried over magnesium sulfate and concentrated in vacuo to afford a beige solid (10.5 g). The crude material was further purified by silica gel flash column chromatography using hexane-ethyl acetate (1:1) as the eluent to give the purified title compound as a white solid (9.77 g, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05922872
Source datasetuspto-grants-1999_07
ORD IDord-f6da1836ccf545748c5c91192334a9d9
Source noteuspto-grants-1999_07