Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38708Generated: October 26, 2026

Chloroacetanilide → HCID 178457010, compound

https://huagongshe.com/reaction/38708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetanilideHCID 11485—
ReactantSodium hydrideHCID 24758—
ReactantPropyl IsothiocyanateHCID 69403—
ReactantDiethylether hexaneHCID 21584099—
SolventDimethylformamideHCID 6228—
ProductHCID 178457010HCID 178457010—

Reaction Steps

At rt, NaH (154 mg of 55% dispersion in mineral oil, 3.54 mmol) is added in portions to a solution of n-propylisothiocyanate (596 mg, 5.90 mmol) and the above 2-chloro-N-phenyl-acetamide (1000 mg, 5.90 mmol) in DMF (30 mL). Stirring is continued for 2 h after completion of the addition. The mixture is poured onto EA (150 mL) and is extracted twice with 1 N aq. HCl (200 mL). The aq. layer is neutralised by adding 3 N NaOH followed by sat. aq. NaHCO3, and extracted twice with EA (200 mL). The organic extracts are washed with water (200 mL) and evaporated to give a pale yellow, crystalline solid. This material is suspended in a small amount of diethyl ether/hexane 1:1, filtered, washed with additional diethyl ether/hexane and dried under high vacuum to give 3-phenyl-2-[(Z)-propylimino]-thiazolidin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524752B2
Source datasetuspto-grants-2013_09
ORD IDord-5de96110d2c3432d9c3ed8270c8244a2
Source noteuspto-grants-2013_09