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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128349Generated: October 30, 2026

Triethylamine → HCID 23469427, compound

https://huagongshe.com/reaction/128349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAcryloyl chlorideHCID 13140—
ReactantN-[(4-Hydroxyphenyl)methyl]methanesulfonamideHCID 17825897—
SolventDichloromethaneHCID 6344—
ProductHCID 23469427HCID 23469427—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 20.1 g (0.10 mol) of N-(4-hydroxybenzyl)methanesulfonamide, 10.1 g (0.10 mol) of triethylamine and 100 ml of methylene chloride cooled to approximately 0° C. was added a solution of 9.0 g (0.10 mol) of acryloyl chloride in 50 ml of methylene chloride over a 10-minute period. Stirring was continued for 30 minutes, and the mixture was filtered. The filtrate was washed twice with water, dried over magnesium sulfate and concentrated in a rotary evaporator. The residue was recrystallized from 100 ml of 1:1 hexane:1,2-dichloroethane. The yield of N-(4-acryloyloxybenzyl)methanesulfonamide was 8.2 g (32.1 percent of theory), m.p.=112° to 115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04259469
Source datasetuspto-grants-1981_03
ORD IDord-eefc0a97718144d2871cb6b043666ec1
Source noteuspto-grants-1981_03