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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419838Generated: November 2, 2026

Dichloromethane → trans-Thiothixene

https://huagongshe.com/reaction/2419838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant(Z)-ThiothixeneHCID 941651—
SolventWaterHCID 962—
Producttrans-ThiothixeneHCID 941650100%

Reaction Steps

5N aqueous sodium hydroxide was added to a suspension of thiothixene.2H3PO4 (63.96 g., 100 mmoles, ca. 85% trans/ 15% cis) in water (750 ml.)/methylene chloride (750 ml.) until the aqueous phase was strongly basic. The phases were separated and the aqueous phase extracted with an additional 200 ml. portion of methylene chloride. The combined methylene chloride extract was dried (Na2SO4), filtered and evaporated in vacuo to a light brown oil (ca. 45 g., ca. 100% yield, ca. 85% trans/15% cis). The oil was dissolved in warm acetonitrile (100 ml.) and the solution cooled to room temperature. Some solids, probably trans-thiothixene, formed upon cooling. Potassium t-butoxide (1.1 g., 9.8 mmoles) was added and the mixture stirred overnight at room temperature. Analysis of the reaction mixture, which contained solids, showed a ca. 85% cis/ 15% trans ratio of isomers. Water (10 ml.) was then added and the reaction mixture stirred briefly at room temperature. The tan cis-thiothixene solids were then filtered, washed with acetonitrile, and dried (35.0 g., 78.9% yield, 5% trans, m.p. 143°-145° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107430
Source datasetuspto-grants-1978_08
ORD IDord-803b0ce254dc4d0382c2655ea3f960df
Source noteuspto-grants-1978_08