HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482615Generated: October 31, 2026
Methanethiol → 1-(4-Chlorophenyl)-2-(methylsulfanyl)ethan-1-one
https://huagongshe.com/reaction/482615
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | p-Chlorophenacyl bromide | HCID 68303 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Chlorophenyl)-2-(methylsulfanyl)ethan-1-one | HCID 14373033 | 97% |
Reaction Steps
To 11.3 g (141 mmole) of 50% aqueous sodium hydroxide dissolved in 50 ml of methanol and cooled to -20° C. was added 7.7 g (160 mmole) of gaseous methyl mercaptan. To this solution was added 30.5 g (130 mmole) of 2-bromo-4'-chloroacetophenone dissolved in 40 g of tetrahydrofuran. After warming to room temperature and stirring for 30 minutes the mixture was concentrated in vacuo, partitioned between hexanes and water, dried over anhydrous magnesium sulfate, filtered, and reconcentrated in vacuo to yield 25.3 g of 2-methylthio-4'-chloroacetophenone, an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05798311 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-28cd0e0b900649d0881b1d79446772e3 |
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| Source note | uspto-grants-1998_08 |
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