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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128343Generated: October 30, 2026

Methacryloyl chloride → HCID 18668254, compound

https://huagongshe.com/reaction/128343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethacryloyl chlorideHCID 13528—
ReactantN-(2-hydroxyphenyl)methanesulfonamideHCID 316696—
SolventDichloromethaneHCID 6344—
ProductHCID 18668254HCID 18668254—

Reaction Steps

To a solution of 10.12 g (0.10 mol) of triethylamie, 18.72 g (0.10 mol) of N-(2-hydroxyphenyl)methanesulfonamide and 300 ml of methylene chloride cooled to 0° C. was added a solution of 10.45 g (0.10 mol) of methacryloyl chloride in 100 ml of methylene chloride over a 15-minute period. After stirring 2 hours at reduced temperature, the solution was washed three times with water, dried over magnesium sulfate and concentrated to an oil. On cooling and scratching, the oil crystallized. Recrystallization from 1:1 benzene:hexane gave a white solid which was collected, washed with 1:1 benzene:hexane, and dried at room temperature in vacuo. The yield of N-(2-methacryloyloxyphenyl)methanesulfonamide was 10.4 g (40.7 percent); m.p.=88° to 90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259469
Source datasetuspto-grants-1981_03
ORD IDord-b41cdd2963004bd183a6fbb271b1f286
Source noteuspto-grants-1981_03