HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329397Generated: October 29, 2026
Acetic Acid → 4-(4-(2-Chloroethyl)phenyl)thiazol-2-one
https://huagongshe.com/reaction/329397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | 4'-(beta-Chloroethyl)acetophenone | HCID 144359 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(4-(2-Chloroethyl)phenyl)thiazol-2-one | HCID 15054214 | 68% |
Reaction Steps
To a 125 ml round-bottomed flask equipped with N2 inlet were added 9.1 g (50 mmol) of 4-(2-chloroethyl)acetophenone and 25 ml acetic acid. To the stirred solution was added 2.58 ml (50 mmol) of bromine dropwise over 2 minutes. The reaction was stirred at room temperature for 30 minutes, taken up in ethyl acetate, washed with water, saturated aqueous sodium bicarbonate solution, and brine, dried over sodium sulfate, and evaporated to an oil. The oil was taken up in 250 ml of acetone, treated with 4.9 g (50 mmol) of potassium thiocyanate, and stirred at room temperature for 3 hours. The precipitate was filtered and the filtrate evaporated. The residue was taken up in ethyl acetate, washed with water and brine, dried over sodium sulfate, and evaporated to a solid. The solid was taken up in 100 ml of boiling ethanol and treated slowly with 83 ml of 1N HCl, then refluxed for 14 hours. The reaction was cooled and the precipitate filtered, washed with water, and dried to give 8.2 g (68%) of a white solid, m.p. 226°-229° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04891375 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-cc970eb3794b42dfbd6d7eb504dda213 |
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| Source note | uspto-grants-1990_01 |
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