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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122015Generated: October 27, 2026

Carbon Disulfide → HCID 178474076, compound

https://huagongshe.com/reaction/2122015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DisulfideHCID 6348—
ReactantDimethyl SulfateHCID 6497—
ReactantN-(4-Chloro-3-nitrophenyl)acetamideHCID 79672—
ReactantSulfurHCID 5362487—
SolventWaterHCID 962—
ProductHCID 178474076HCID 17847407655.3%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of Na2S.9H2O (65 g, 0.28 mol), sulfur (25 g, 0.78 mol) and water (150 mL) were heated with stirring at 90° C. for 10 min, and then poured into a flask charged with the above 4′-chloro-3′-nitroacetanilide (21.5 g, 0.10 mol). The resulting mixture was heated at 80° C. for 10 min, and then CS2 (12 mL, 0.2 mol) was added dropwise while maintaining a gentle reflux. The resulting mixture was heated at 90° C. for 7 h. The solids were collected by filtration, washed with water and dilute HCl solution. The solids were taken up in water, and the solution was made alkaline with solid NaOH. The solution was filtered, and the filtrate was acidified with conc HCl. The precipitates were collected by filtration, washed with water, and dried under high vacuum. The crude product was suspended in cold water (200 mL) and solid Na2CO3 was added to obtain pH 13. Dimethyl sulfate was added to the above milky solution, and the resulting mixture was stirred at ambient temperature for 3 h. The solids were collected by filtration, washed with water, and dried under high vacuum to yield the title compound (12.4 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696473B2
Source datasetuspto-grants-2004_02
ORD IDord-29645c8bb44a402cb729dafa5ef72e89
Source noteuspto-grants-2004_02