HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461160Generated: October 26, 2026
Hydrochloric Acid → 2-Chloro-4'-isopropyl-3'-sulfamoylacetophenone
https://huagongshe.com/reaction/461160
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | 2-(2-Hydroxyethoxy)ethanol;methoxymethane | HCID 21225657 | — |
| Reactant | 4-Isopropyl-3-sulfamoylbenzoylchloride | HCID 22760505 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Chloro-4'-isopropyl-3'-sulfamoylacetophenone | HCID 22760666 | — |
Reaction Steps
13.5 g of 4-isopropyl-3-sulfamoylbenzoyl chloride were reacted as prescribed in Example 66b) with diazomethane in ether, the 4'-isopropyl-3'-sulfamoyldiazoacetophenone remaining in solution without precipitating as crystals. The solution so obtained was allowed to flow into a mixture of 200 ml of diethylene glycol-dimethyl ether and 100 ml of concentrated hydrochloric acid while stirring and cooling with ice, whereafter the solvent was largely distilled off under reduced pressure. To the oily residue, 500 ml of water were added and the solution was extracted with 200 ml of ethyl acetate. Drying followed over sodium sulfate and the solvent was distilled off under reduced pressure. The oily residue crystallized in the course of 1 to 3 days and was then triturated under a small amount of xylene and filtered off. Melting point: 141° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04061761 |
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| Source dataset | uspto-grants-1977_12 |
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| ORD ID | ord-37e224dcd70c4c6da65028c3c514d833 |
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| Source note | uspto-grants-1977_12 |
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