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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413826Generated: November 2, 2026

Thiophenol → HCID 70577630, compound

https://huagongshe.com/reaction/1413826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
Reactant3-Benzyl-6-oxa-3-azabicyclo(3.1.0)hexaneHCID 9815370—
CatalystWaterHCID 962—
ProductHCID 70577630HCID 70577630—

Reaction Steps

A mixture of 8.8 g. (0.05 mole) of 1-benzyl-3,4-epoxypyrrolidine, 6.0 g. (0.055 mole) of thiophenol, and 3 drops of water was heated on a steam bath overnight. Upon cooling the mixture, a solid crystallized. The solid was dissolved in methylene chloride and the methylene chloride solution was washed with two 50-ml portions of 5% sodium hydroxide. The methylene chloride layer was dried over anhydrous sodium sulfate and concentrated to give a yellow oil which solidified on standing. The solid was recrystallized from cyclohexane to give 8.6 g. (60%) of a tan solid, m.p. 97°-99°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251541
Source datasetuspto-grants-1981_02
ORD IDord-8b3209f6e18046819d951319c4dd9b9e
Source noteuspto-grants-1981_02