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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977952Generated: October 30, 2026

Carbon Disulfide → ethyl 2-(1,3-dithiol-2-ylidene)-2-(N-benzylcarbamoyl)acetate

https://huagongshe.com/reaction/977952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantPotassium HydroxideHCID 14797—
Reactantcis-1,2-DichloroethyleneHCID 643833—
ReactantEthyl 3-(benzylamino)-3-oxopropanoateHCID 11379032—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Productethyl 2-(1,3-dithiol-2-ylidene)-2-(N-benzylcarbamoyl)acetateHCID 2020401962.8%

Reaction Steps

Ethyl (N-benzylcarbamoyl)acetate (39.00 g) and carbon disulfide (14.03 g) are dissolved in dimethylsulfoxide (390 ml). A solution of potassium hydroxide (21.52 g) in water (39 ml) is added dropwise to the mixture at 20° to 40° C. The mixture is stirred at the same temperature for 30 minutes, and then cis-1,2-dichloroethylene (17.84 g) is added dropwise thereto. The mixture is stirred at 50° C. for 5 hours. Cis-1,2-dichloroethylene (3.24 g) is further added to the mixture 3 hours after the commencement of the reaction. After cooling, the mixture is poured into water, and the aqueous solution is extracted with ethyl acetate. The extract is washed with water, dried and then evaporated to remove the solvent. The residue is purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate=2:1), and then recrystallized from a mixture of n-hexane and ethyl acetate, whereby ethyl 2-(1,3-dithiol-2-ylidene)-2-(N-benzylcarbamoyl)acetate (33.77 g) is obtained as pale yellow prisms. Yield: 62.8%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04663319
Source datasetuspto-grants-1987_05
ORD IDord-cd08dec0f9c14a658a70021c9cba4417
Source noteuspto-grants-1987_05