HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methacryloyl chloride → HCID 18668254, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | N-(2-hydroxyphenyl)methanesulfonamide | HCID 316696 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18668254 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259469 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-b41cdd2963004bd183a6fbb271b1f286 |
| Source note | uspto-grants-1981_03 |