HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111525Generated: November 1, 2026
Ethanone, 1-(3,4-dichlorophenyl)- → 1-(3-Chloro-4-mercapto-phenyl)ethanone
https://huagongshe.com/reaction/1111525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanone, 1-(3,4-dichlorophenyl)- | HCID 75841 | — |
| Reactant | Sodium hydrogen sulphide | HCID 86586439 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(3-Chloro-4-mercapto-phenyl)ethanone | HCID 14365371 | 90.7% |
Reaction Steps
110 g (1.48 mol) of sodium hydrogen sulphide (NaSH·H2O) are initially introduced together with 1 l of N-methylpyrrolidone and the water is removed at 160° C. with nitrogen. The mixture is cooled to 140° C. and 112 g (0.59 mol) of 3,4-dichloroacetophenone are added, and the mixture is reacted further at 160° C. for 3 hours, and N-methylpyrrolidone is distilled off. The residue is taken up in 1 l of water and filtered, and the filtrate is acidified at 0°-10° C. with half-concentrated hydrochloric acid. The precipitate is filtered off with suction, washed neutral and dried. Distillation under reduced pressure gives 99.8 g (90.7% of theory) of 2-chloro-4-acetylthiophenol of boiling point: 125°-130° C./0.1 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04980510 |
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| Source dataset | uspto-grants-1990_12 |
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| ORD ID | ord-3bc5b4db269b44bcb7c9007dba606a2a |
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| Source note | uspto-grants-1990_12 |
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