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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128348Generated: October 29, 2026

Triethylamine → HCID 23469426, compound

https://huagongshe.com/reaction/128348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethacryloyl chlorideHCID 13528—
ReactantN-[(4-Hydroxyphenyl)methyl]methanesulfonamideHCID 17825897—
SolventDichloromethaneHCID 6344—
ProductHCID 23469426HCID 23469426—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 6.04 g (0.03 mol) of N-(4-hydroxybenzyl)methanesulfonamide, 3.04 g (0.03 mol) of triethylamine, and 30 ml of methylene chloride was cooled to approximately 0° C. To this mixture was added a solution of 3.14 g (0.03 mol) of methacryloyl chloride in 15 ml of methylene chloride over approximately 5 minutes. The mixture was stirred for an additional 15 minutes and filtered. The filtrate was washed twice with water, dried over magnesium sulfate and concentrated in a rotary evaporator. The solid residue was recrystallized from 1:1 hexane:1,2-dichloroethane. The yield of N-(4-methacryloyloxybenzyl)methanesulfonamide was 3.0 g (37.13 percent of theory), m.p.=101° to 102.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259469
Source datasetuspto-grants-1981_03
ORD IDord-4ffd12e686464993a8b006dd3d649006
Source noteuspto-grants-1981_03