HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885563Generated: October 27, 2026
2-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-one → 2-Acetylaminomethyl-4,5-bis(4-methoxyphenyl)thiazole
https://huagongshe.com/reaction/1885563
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Chloro-1,2-bis(4-methoxyphenyl)ethan-1-one | HCID 3862523 | — |
| Reactant | N-(2-amino-2-thioxoethyl)acetamide | HCID 4435531 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Acetylaminomethyl-4,5-bis(4-methoxyphenyl)thiazole | HCID 10044540 | 33.2% |
Reaction Steps
A mixture of 1,2-bis(4-methoxyphenyl)-2-chloroethanone (5.99 g) and 2-(acetylamino)ethanethioamide (3.00 g) in ethanol (30 ml) was refluxed for 2 hours. After allowing to cool to room temperature, the solvent was evaporated in vacuo, and the residue was dissolved in chloroform (200 ml) and aqueous solution of sodium hydrogencarbonate (200 ml). The separated organic layer was washed with water and brine, dried over magnesium sulfate and treated with activated charcoal. After filtration, the filtrate was evaporated in vacuo. The resulting residue was dissolved in diethyl ether, added ethanol solution of hydrogen chloride, and the resulting precipitate was collected by filtration. The resulting crude compound was recrystallized with ethanol 10 ml). And the resulting crystal was collected by filtration, washed with ethanol and diethyl ether, and dried to give 2-acetylaminomethyl-4,5-bis(4-methoxyphenyl)thiazole (2.52 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05145860 |
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| Source dataset | uspto-grants-1992_09 |
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| ORD ID | ord-3e32c6f498b947fe96955056dc62ee99 |
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| Source note | uspto-grants-1992_09 |
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