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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581903Generated: October 25, 2026

Benzyl Chloride → N-benzyl-thiazolinethion

https://huagongshe.com/reaction/1581903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant2-Benzylthio-2-thiazolineHCID 275677—
SolventMethanolHCID 887—
ProductN-benzyl-thiazolinethionHCID 125489430704.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

12.7 g (0.1 mole) of benzylchloride were added to 209.2 g (1 mole) of 2-benzylthio-thiazoline and the mixture was heated to 150° C. for eight hours. The mixture was allowed to cool down to 70° C. and 500 ml of methanol were added. The reaction mixture was allowed to cool down to room temperature and stirred for an additional hour; N-benzyl-thiazoline-thion precipitated from the medium as a white crystalline product, was isolated by filtration and washed twice with 10 ml of methanol. The crude product was recrystallized from a minimum of acetonitrile. 146 g of N-benzyl-thiazolinethion were isolated and sulfonated as described below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06733947B2
Source datasetuspto-grants-2004_05
ORD IDord-789ad516cc7a459dbf3e7dacc4f95292
Source noteuspto-grants-2004_05