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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259435Generated: November 1, 2026

Allyl bromide → HCID 54396564, compound

https://huagongshe.com/reaction/2259435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantTriethylamineHCID 8471—
ReactantHCID 3937474HCID 3937474—
SolventEthanolHCID 702—
ProductHCID 54396564HCID 5439656480%

Reaction Steps

11.0 g (90 mmol) of allyl bromide were added to 10.0 g (44.8 mmol) of N-cinnamylbenzylamine in 60 ml of ethanol, and then 5.0 g (50.0 mmol) of triethylamine were added while stirring. The mixture was refluxed for 4 h. Concentration under water pump vacuum was followed by partition of the contents of the flask between methylene chloride and water, rendition alkaline with dilute sodium hydroxide solution and extraction twice more with methylene chloride. The combined organic phases were washed with dilute sodium hydroxide solution, dried and concentrated. The crude product (12.5 g) was purified by column chromatography (silica gel, mobile phase methylene chloride/methanol 98/2). 9.2 g (80%) of product (oil) were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05473080
Source datasetuspto-grants-1995_12
ORD IDord-01fd0d74c336487db5ec272954bc21ce
Source noteuspto-grants-1995_12