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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419567Generated: November 3, 2026

3-[(1,3-Benzodithiol-2-ylidene)amino]-2-thioxo-4-thiazolidinone → 3-[(1,3-Benzodithiol-2-ylidene)amino]-5-pentylidene-2-thioxo-4-thiazolidinone

https://huagongshe.com/reaction/2419567

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(1,3-Benzodithiol-2-ylidene)amino]-2-thioxo-4-thiazolidinoneHCID 12494993—
CatalystPiperidine, acetateHCID 9793820—
SolventPentanalHCID 8063—
Product3-[(1,3-Benzodithiol-2-ylidene)amino]-5-pentylidene-2-thioxo-4-thiazolidinoneHCID 5732453289.6%

Reaction Steps

A slurry of 2.0g of 3-[(1,3-benzodithiol-2-ylidene)amino]- 2-thioxo-4-thiazolidinone (see example 37), valeraldehyde (10 ml, excess) and acetic acid/piperidine (2:1) (10 drops) in anhydrous slyme (400 ml) is heated at reflux for eighteen hours. The reaction mixture is chilled in an ice bath and the resultant precipitate collected by filtration. This precipitate (1.6 g) is recrystallized from 50 ml of dimethylformamide to yield 1.1 g of the title compound, melting point 210°-212° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04107175
Source datasetuspto-grants-1978_08
ORD IDord-ee6cda9cab894396a20a06a768418928
Source noteuspto-grants-1978_08