HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372640Generated: October 30, 2026
Methanesulfonyl chloride → HCID 22203276, compound
https://huagongshe.com/reaction/2372640
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Veratrylamine | HCID 79832 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22203276 | HCID 22203276 | — |
Reaction Steps
1-(Aminomethyl)-3,4-dimethoxybenzene (18 ml., 120 mmole, 2 eq.) was added to a solution of methanesulfonyl chloride (4.64 ml., 60 mmole, 1 eq.) in dichloromethane (30 ml., 2.0M) at 0°. Additional dichloromethane (90 ml., final concentration of 0.5M) was then added. The reaction was allowed to warm to room temperature and stirred 2 days. The solid which had precipitated was filtered off and washed with additional dichloromethane. The filtrate was washed with 0.5N HCl (2×200 ml.) and water (200 ml.), dried (MgSO4), filtered, and concentrated to give 13.93 g. of yellow solid. This material was recrystallized from ethyl acetate:hexane (1:1, 75 ml.). The crystalline product was washed with ethyl acetate:hexane (1:1) and ether and dried to give 12.41 g. of N-[(3,4-dimethoxy)methyl]methanesulfonamide; m.p. 78°-81°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098924 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-f00436c8e76b408381b6a6e7bb7e7782 |
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| Source note | uspto-grants-1992_03 |
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