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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206660Generated: November 2, 2026

Epichlorohydrin → Bis(3-chloro-2-hydroxypropyl)sulfide

https://huagongshe.com/reaction/2206660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactant1-Chloro-3-mercapto-2-propanolHCID 110861—
ProductBis(3-chloro-2-hydroxypropyl)sulfideHCID 19980843—

Reaction Steps

Epichlorohydrin (5563 g, 60.12 mol) and methanol (2500 g) were put into a 10-liter reactor. The reaction temperature was adjusted to 6° C. When the reaction temperature reached 6° C., sodium hydroxide (50% aq., 5 g) was added to the mixture. NaSH.xH2O (70% NaSH, 3660 g, 45.75 mol), methanol (1000 g) and water (500 g) were completely dissolved with stirring in another 10-liter reactor, and hydrochloric acid was slowly added dropwise thereto to generate hydrogen sulfide gas. The hydrogen sulfide gas was added to the epichlorohydrin solution to obtain bis(3-chloro-2-hydroxypropyl)sulfide. The completion of the reaction was defined as the time when epichlorohydrin and 3-chloro-2-hydroxy-propane-1-thiol disappeared completely and bis(3-chloro-2-hydroxypropyl)sulfide was formed, which was confirmed by GC. When 3-chloro-2-hydroxy-propane-1-thiol was present, the content of the thiol compound was calculated from the relative integral ratio by GC and epichlorohydrin was further added in an amount corresponding to the calculated content. The reaction of epichlorohydrin and the thiol compound afforded bis(3-chloro-2-hydroxypropyl)sulfide (BCPS).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09372281B2
Source datasetuspto-grants-2016_06
ORD IDord-c03302e9cb014f0a9f42bc0faf68489b
Source noteuspto-grants-2016_06