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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198221Generated: November 1, 2026

Diethyl Ether → (2S)-2-[4-(benzyloxy)phenyl]oxirane

https://huagongshe.com/reaction/1198221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium HydroxideHCID 14797—
Reactant(S)-1-(4-benzyloxyphenyl)-2-bromoethanolHCID 11716484—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(2S)-2-[4-(benzyloxy)phenyl]oxiraneHCID 2284995967.9%

Reaction Steps

2.8 g of (S)-1-(4-benzyloxyphenyl)-2-bromoethanol was dissolved in a mixed solvent of 20 ml of methanol and 10 ml of tetrahydrofuran. To the solution was added a solution of 0.8 g of potassium hydroxide dissolved in 4 ml of water, with ice cooling. The mixture was stirred for 5 minutes at the same temperature and further for 10 minutes at room temperature. The reaction mixture was added to a mixture of 50 ml of diethyl ether and 50 ml of ice water. The organic layer was separated. The aqueous layer was extracted with 25 ml of diethyl ether. The extract was combined with the previously separated organic layer. The combined organic layer was washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 1.4 g of (S)-2-(4benzyloxyphenyl)oxirane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05280032
Source datasetuspto-grants-1994_01
ORD IDord-ce733a4c378049d7a6c08ae58614c9d1
Source noteuspto-grants-1994_01