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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206662Generated: October 26, 2026

Acetic Anhydride → 1,1'-Thiobis(2,3-epithiopropane)

https://huagongshe.com/reaction/2206662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium HydroxideHCID 14798—
ReactantThioureaHCID 2723790—
ReactantBis(3-chloro-2-hydroxypropyl)sulfideHCID 19980843—
Reactant2,3-Epoxypropyl(2,3-epithiopropyl)sulfideHCID 87739564—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product1,1'-Thiobis(2,3-epithiopropane)HCID 10976066—

Reaction Conditions

Temperature36 °C

Reaction Steps

1072.48 g (8.47 mol) of bis(3-chloro-2-hydroxypropyl)sulfide, 1300 g of toluene, and 800 g of methanol were put into a 10-liter reactor. The reaction temperature was adjusted to 30° C. with stirring. When the reaction temperature reached 25° C., NaOH (50% aq., 783.08 g, 9.78 mol) was added dropwise within 1 h. The reaction was carried out while maintaining a temperature of 35-37° C. After standing at 37° C. for about 30 min, 2000 g of toluene was added to the reaction mixture, followed by stirring for about 10 min. The resulting mixture was left standing for layer separation. The upper organic layer was washed twice with water, and then the water was removed as much as possible. To the organic layer was added 400 g of methanol. After stirring, thiourea (1117.65 g, 14.30 mol) and acetic anhydride (70 g) were added at a temperature of 8° C. The reaction was continued at 18° C. for 18 h. The reaction was stopped when almost all the starting materials disappeared, which was confirmed by HPLC, and the content of 2,3-epoxypropyl(2,3-epithiopropyl)sulfide reached 6%, which was confirmed by GC analysis. After completion of the reaction, stirring was stopped for layer separation. The obtained organic layer was washed three times with water and the organic solvent was removed, affording bis(2,3-epithiopropyl)sulfide. The product had a refractive index (nD, 20° C.) of 1.618.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09372281B2
Source datasetuspto-grants-2016_06
ORD IDord-2a572ac447524c1f92b50e2165224176
Source noteuspto-grants-2016_06