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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078091Generated: October 31, 2026

Methanesulfonyl chloride → HCID 22203276, compound

https://huagongshe.com/reaction/1078091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantVeratrylamineHCID 79832—
SolventDichloromethaneHCID 6344—
ProductHCID 22203276HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05545838
Source datasetuspto-grants-1996_08
ORD IDord-9ad20ea1aae24690a7d8054b565efba3
Source noteuspto-grants-1996_08