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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259344Generated: November 1, 2026

Diethyl Ether → (R)-2-(benzo[b]thiophen-5-yl)oxirane

https://huagongshe.com/reaction/2259344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium HydroxideHCID 14797—
Reactant(R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanolHCID 53833740—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-(benzo[b]thiophen-5-yl)oxiraneHCID 2993902979.2%

Reaction Steps

3.5 g of (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol was dissolved in a mixed solvent of 20 ml of methanol and 10 ml of tetrahydrofuran. Thereto was added a solution of 1.5 g of potassium hydroxide dissolved in 5 ml of water, with ice cooling. The resulting 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 60 ml of diethyl ether and 60 ml of ice water. The organic layer was separated. The aqueous layer was extracted with 30 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 1.9 g of (R)-2-(benzo[b]thiophen-5-yl)oxirane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05472984
Source datasetuspto-grants-1995_12
ORD IDord-73f4ef041699484a99362b9fc8650823
Source noteuspto-grants-1995_12