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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862496Generated: October 30, 2026

Diethyl Ether → HCID 11379137, compound

https://huagongshe.com/reaction/862496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 11289766HCID 11289766—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11379137HCID 1137913783.7%

Reaction Steps

6.0 g of (R)-1-(4-benzyloxyphenyl)-2-bromoethanol was dissolved in a mixed solvent of 50 ml of methanol and 25 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 100 ml of diethyl ether and 100 ml of ice water. The organic layer was separated. The aqueous layer was extracted with 50 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 3.7 g of (R)-2-(4-benzyloxyphenyl)oxirane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05719150
Source datasetuspto-grants-1998_02
ORD IDord-c9a5a507863047db921a0a7d70faeaad
Source noteuspto-grants-1998_02