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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1680212Generated: November 1, 2026

Allyl bromide → HCID 12895736, compound

https://huagongshe.com/reaction/1680212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant2-Chloro-5-(chloromethyl)thiopheneHCID 583079—
ReactantHCID 178455850HCID 178455850—
SolventDiethyl EtherHCID 3283—
ProductHCID 12895736HCID 12895736195.9%

Reaction Steps

A solution of allyl magnesium bromide (from 14.6 g of magnesium and 24.2 g (0.2 M) of allyl bromide) in 100 ml ether is added dropwise with stirring to 29.9 g of 5-chloro-2-chloromethylthiophene in 10 ml ether over half an hour and the resulting mixture heated under reflux overnight. The mixture is then poured into 300 ml ice cold dilute sulfuric acid, the ether layer separated and the aqueous phase extracted with 200 ml of ether. The combined ethereal solutions are washed with aqueous potassium carbonate, dried over MgSO4 and evaporated to give crude 4-(5-chloro-2-thienyl)-1-butene as a yellow oil (34 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04272545
Source datasetuspto-grants-1981_06
ORD IDord-11bf73e510b5456ba3a8bad29c96dd32
Source noteuspto-grants-1981_06