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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973324Generated: November 2, 2026

Bromoacetyl bromide → Acetamide, 2-bromo-N-methyl-N-2-propynyl-

https://huagongshe.com/reaction/1973324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromoacetyl bromideHCID 61147—
ReactantN-methylpropyn-2-ylamineHCID 96160—
ReactantSodium BicarbonateHCID 516892—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductAcetamide, 2-bromo-N-methyl-N-2-propynyl-HCID 1077401885%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 13.8 g (0.2 mol) of N-methylpropargylamine in 20 ml methylene chloride was added dropwise to a stirred and cooled (below 15° C) solution of 40.2 g (0.2 mol bromoacetyl bromide and 16 g (0.2 mol) sodium bicarbonate in 250 ml methylene chloride. The reaction mixture was allowed to warm to about 25° C and stirred for 2 hours. The reaction mixture was then filtered and evaporated under reduced pressure to give an oily residue. The residue was diluted with 150 ml ethyl ether to form a two-phase mixture consisting of an ether phase and a dark oil. The ether phase was separated, dried over magnesium sulfate, and evaporated to give 32.3 g of N-methyl-N-propargyl-alpha-bromoacetamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997326
Source datasetuspto-grants-1976_12
ORD IDord-87137ed9e7814607b0e727ce3196f3a8
Source noteuspto-grants-1976_12