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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 462445Generated: October 30, 2026

Allyl bromide → 3-(Prop-2-en-1-yl)benzaldehyde

https://huagongshe.com/reaction/462445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-BromobenzaldehydeHCID 76583—
ReactantMagnesiumHCID 5462224—
SolventCarbon DioxideHCID 280—
SolventTetrahydrofuranHCID 8028—
Product3-(Prop-2-en-1-yl)benzaldehydeHCID 22022690101.3%

Reaction Steps

The ethylene acetal of 3-bromobenzaldehyde (10 g) is converted into the Grignard reagent by reaction with magnesium (1.13 g) in dry THF (ca. 250 ml). Cuprous bromide (0.9 g) is added and the mixture is cooled in cardice. Allylbromide (8.52 g) in dry THF is then added and the mixture is stirred overnight following which saturated ammonium chloride is added, the mixture is extracted with diethyl ether (3 times), the ether extract is washed, dried and the solvent evaporated to yield the crude ethylene acetal of 3-allylbenzaldehyde (8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04515808
Source datasetuspto-grants-1985_05
ORD IDord-6aae9a641d6640b5a687d8b7d3b7c259
Source noteuspto-grants-1985_05