HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879501Generated: October 25, 2026
Chloroacetanilide → HCID 178457010, compound
https://huagongshe.com/reaction/1879501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetanilide | HCID 11485 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Propyl Isothiocyanate | HCID 69403 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178457010 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE043833E1 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-2d1c882bbac34d7db5996546e50d7722 |
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| Source note | uspto-grants-2012_11 |
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