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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2371915Generated: October 31, 2026

Ethyl Bromide → HCID 131717191, compound

https://huagongshe.com/reaction/2371915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-EthynylthiopheneHCID 5246258—
ReactantMagnesiumHCID 5462224—
ReactantEthanone, 2-chloro-1-(1-chlorocyclopropyl)-HCID 11062580—
SolventDiethyl EtherHCID 3283—
ProductHCID 131717191HCID 13171719197.3%

Reaction Steps

22.2 g (0.203 mole) of ethyl bromide are slowly added to 4.9 g (0.203 mole) of magnesium turnings in 100 ml of diethyl ether. After completion of the addition, the reaction mixture is heated under reflux for 30 minutes and then cooled to room temperature, and a solution of 20 g (0.185 mole) of 2-thienylethine in 50 ml of diethyl ether is subsequently added dropwise with stirring. The mixture is heated under reflux for 1 hour and again cooled to room temperature. 28.3 g (0.185 mole) of 1-chloro-cyclopropyl chloromethyl ketone are added dropwise with stirring and the mixture is then heated under reflux for a further 2 hours. After cooling to room temperature, the reaction mixture is poured into a saturated aqueous ammonium chloride solution and the mixture is extracted three times with diethyl ether. The combined organic phases are washed once with water, dried over sodium sulphate and concentrated under reduced pressure. 47.0 g (97% of theory) of 1-chloro-2-(1-chloro-cyclopropyl)-4-(thiophen-2-yl)-but-3-in-2-ol are obtained in this way in the form of an oil which is reacted further without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05096912
Source datasetuspto-grants-1992_03
ORD IDord-a8c57d338b6c45b795d6aebe1c07ca73
Source noteuspto-grants-1992_03