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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263030Generated: November 3, 2026

N-bromobutanimide → Ethyl 6-bromo-2,3,3-trimethylhex-4-enoate

https://huagongshe.com/reaction/1263030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl 2,3,3-trimethylhex-4-enoateHCID 54109182—
CatalystBenzoyl PeroxideHCID 7187—
SolventCarbon TetrachlorideHCID 5943—
ProductEthyl 6-bromo-2,3,3-trimethylhex-4-enoateHCID 5443703986.6%

Reaction Steps

A mixture of 920 mg (5 mmoles) of ethyl 2,3,3-trimethyl-4-hexenoate, 10 ml of carbon tetrachloride, 107 mg (6 mmoles) of N-bromosuccinimide, and 50 mg of benzoyl peroxide was heated under reflux for about two hours. The insoluble succinimide was removed by filtration. The filtrate was washed successively with saturated aqueous sodium bicarbonate solution and water, then dried over magnesium sulfate. The dried solution was distilled to give 1.14 g (86% yield) of ethyl 6-bromo-2,3,3-trimethyl-4-hexenoate, b.p. 80°-81°/0.8 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04454343
Source datasetuspto-grants-1984_06
ORD IDord-c2756fa178394c659e661471ff4bca06
Source noteuspto-grants-1984_06