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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 443046Generated: October 30, 2026

Epichlorohydrin → Tert-octylglycidyl thioether

https://huagongshe.com/reaction/443046

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactanttert-OCTYL MERCAPTANHCID 8851—
ReactantSodium HydroxideHCID 14798—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
ProductTert-octylglycidyl thioetherHCID 85528098—

Reaction Steps

A solution of 66 parts by weight of sodium hydroxide, 300 parts by weight of water and 8 parts by weight of tetrabutylammonium chloride is added dropwise at 15° to 20° C. in the course of 70 minutes, with stirring and partial cooling (especially at the commencement of the addition), to a mixture of 219 parts by weight of tert-octylmercaptan and 135 parts by weight of epichlorohydrin. The reaction mixture is further stirred for 1 hour at 50° C.; the aqueous phase is then separated, and the organic phase is washed with 200 parts by weight of water. The organic phase is finally distilled in vacuo to thus obtain the tert-octylglycidyl thioether in the form of a colourless liquid having a boiling point of 74° to 75° C. at 0.02 mbar, and a refractive index of nD20 =1.4803; the yield is 250 parts by weight, which corresponds to 82% of the theoretical yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05892051
Source datasetuspto-grants-1999_04
ORD IDord-8173d694907c48ed97bf5ac890961f27
Source noteuspto-grants-1999_04