HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881243Generated: October 26, 2026
Hydrochloric Acid → 2-(Chloromethylsulfonylamino)acetophenone
https://huagongshe.com/reaction/1881243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Chloromethyl)sulfonyl chloride | HCID 77054 | — |
| Reactant | Ethanone, 2-amino-1-phenyl-, hydrochloride (1:1) | HCID 2723597 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(Chloromethylsulfonylamino)acetophenone | HCID 23024417 | 76% |
Reaction Steps
2-Aminoacetophenone hydrochloride (4.56 g, 26.6 mmol) was dissolved in dichloromethane (250 mL). To the solution was added triethylamine (9.30 mL, 66.7 mmol), and the mixture was stirred at room temperature for 10 minutes. After the reaction mixture was cooled to 0° C., chloromethanesulfonyl chloride (purity 90%, 3.60 mL, 36.3 mmol) was added, and the mixture was stirred at the same temperature for 1 hour. To the reaction mixture was added 2 mol/L hydrochloric acid, and the mixture was extracted with chloroform. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. To the residue was added diethyl ether, and the deposited crystals were collected by filtration and dried to give 2-(chloromethylsulfonylamino)acetophenone (5.00 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318782B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-34253188ebc74a5da1ef30c9c7100861 |
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| Source note | uspto-grants-2012_11 |
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