HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 342747Generated: October 31, 2026
Methanesulfonyl chloride → HCID 54083760, compound
https://huagongshe.com/reaction/342747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 54349857 | HCID 54349857 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 54083760 | HCID 54083760 | 63% |
Reaction Steps
N-(1',1'-dimethyl-3'-hydroxyacetonyl)-3,5-dichlorobenzamide (1.0 gm, 0.00345 m) was dissolved in methylene chloride (25 ml) and diisopropylethylamine (0.44 gm, 0.0035 m) and cooled to about 5° C. under a nitrogen atmosphere. While the solution was stirred magnetically, methanesulfonylchloride (0.475 gm, 0.0041 m) was added dropwise. After its addition, the mixture was stirred about an hour longer while maintaining the temperature at 5°-10° C. The mixture was then poured into ice water (500 ml) containing methylene chloride (100 ml). The organic layer was separated and was washed with cold 1% hydrochloric acid, saturated sodium bicarbonate, water and brine, and then dried over anhydrous potassium carbonate. The solvent was removed and 800 mg of the desired product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05859063 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-a2b066b84b704b32bc51d8721a2005ce |
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| Source note | uspto-grants-1999_01 |
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