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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380584Generated: November 3, 2026

Hydrochloric Acid → 2-[(4-Ethylphenyl)methyl]oxirane

https://huagongshe.com/reaction/1380584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEpichlorohydrinHCID 7835—
Reactant1-Bromo-4-ethylbenzeneHCID 15313—
ReactantMagnesiumHCID 5462224—
SolventDiethyl EtherHCID 3283—
Product2-[(4-Ethylphenyl)methyl]oxiraneHCID 23325579—

Reaction Conditions

Temperature20 °C

Reaction Steps

A Grignard solution freshly prepared from 12.15 g (0.50 g atom) magnesium chips and 92.5 g (0.50 mole) 1-bromo-4-ethylbenzene in 400 ml dry ether is dripped with agitation into a precooled solution of 92.5 g (1.00 mole) of epichlorohydrin in 100 ml of dry ether, so that the temperature does not exceed -40° C. After addition is complete, the solution is heated slowly to 20° C. and is hydrolyzed after another three hours by the addition of ice water and dilute hydrochloric acid. The ether phase is separated, washed twice with water and dried over sodium sulfate. Following the removal of the ether, the bath temperature is raised to 70° C. and the volatile components carefully removed at 0.1 mbar. The residue is taken up in 185 ml of methanol and a freshly prepared solution of 6.90 g (0.30 g atom) sodium in methanol added at room temperature. After three hours the sodium chloride precipitate is separated, the filtrate concentrated in vacuum and the yellow, oily residue used without purification for further conversion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582857
Source datasetuspto-grants-1986_04
ORD IDord-a51207bdfb82423c895d29cbedc5ed51
Source noteuspto-grants-1986_04