HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390267Generated: October 31, 2026
N-Methylcyclohexylamine → N-cyclohexyl-N-methylethenesulfonamide
https://huagongshe.com/reaction/390267
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Ethanesulfonylchloride, 2-chloro- | HCID 15385 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-cyclohexyl-N-methylethenesulfonamide | HCID 58625116 | — |
Reaction Steps
A mixture of N-methylcyclohexylamine (0.048 mol) and TEA (0.053 mol) in DCM (200 mL) was cooled in an ice bath to 5° C., and then a solution of 2-chloro-ethanesulfonyl chloride (0.048 mol, 97%) in DCM (20 mL) was added dropwise. The reaction mixture was stirred for 2 hours at room temperature and then was washed with H2O. The organic layer was separated, dried (MgSO4), and filtered, and the solvent was evaporated to yield the title compound as a residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08383637B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-fb74971357bc4d2aaff209748951fcd0 |
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| Source note | uspto-grants-2013_02 |
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