HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258397Generated: October 28, 2026
Chloroacetone → 2-Acetylbenzo[b]thiophene
https://huagongshe.com/reaction/258397
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | 2-Chlorobenzaldehyde | HCID 6996 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 2-Acetylbenzo[b]thiophene | HCID 89805 | 74% |
Reaction Steps
To a 200 ml four-necked flask, equipped with a stirrer, a thermometer and a reflux condenser, were added 11.7 g (150 m moles) of anhydrous sodium sulfide, 3.2 g (100 m moles) of sulfur and 100 ml of N-methylpyrrolidone, and the mixture was stirred at room temperature for one hour. To the reaction mixture was dropwise added 14.1 g (100 m moles) of 2-chlorobenzaldehyde, and the mixture was stirred at room temperature for 12 hours. To the reaction mixture, was dropwise added 11.1 g (120 m moles) of chloroacetone with cooling, and the reaction mixture was stirred at room temperature for 6 hours. After finishing the reaction, 100 ml of diethyl ether and 100 ml of water were added to the reaction mixture, and pH value of the aqueous layer was adjusted to higher than 11 with a sodium hydroxide aqueous solution, and extracted with diethyl ether. The diethyl ether extract was washed twice with water, and the diethyl ether layer was concentrated under a reduced pressure to obtain 13.0 g of 2-acetylbenzo[b]thiophene (yield 74%). Purity of the product was 95% as determined by gas chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05266705 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-179d3449452b4e688d453a963c17d666 |
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| Source note | uspto-grants-1993_11 |
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