Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | N-[(4-Hydroxyphenyl)methyl]methanesulfonamide | HCID 17825897 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23469427 | HCID 23469427 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04259469 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-eefc0a97718144d2871cb6b043666ec1 |
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| Source note | uspto-grants-1981_03 |
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