HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615867Generated: October 25, 2026
Acetone → 2-chloro-N-(4-phenyl-1,3-thiazol-2-yl)propanamide
https://huagongshe.com/reaction/615867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4-phenylthiazole | HCID 40302 | — |
| Reactant | 2-Chloropropionyl chloride | HCID 111019 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-chloro-N-(4-phenyl-1,3-thiazol-2-yl)propanamide | HCID 4558675 | 69.8% |
Reaction Steps
Into 50 ml of acetone, were added 12.5 g of 2-amino-4-phenylthiazole and 7.0 g of triethylamine. The mixture was cooled to -10°--20° C. To the mixture solution, 11.7 g of α-chloropropionylchloride was slowly dropped. After the completion of the dropwise addition, the resultant mixture solution was agitated at room temperature for 3 hours. Then, the reaction mixture was poured into 500 ml of water. Resulting oily substance was extracted with ethyl acetate. The extract was then successively washed with dilute hydrochloric acid and water. After drying the solution, the ethyl acetate was removed under reduced pressure. The residue was recrystallized from an ether/n-hexane mixed solvent to obtain 13.2 g of 2-(α-chloropropionylamino)-4-phenylthiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04501750 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-28740988d9f04efe8a1e08a874dca013 |
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| Source note | uspto-grants-1985_02 |
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