HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → p-Hexadecylamino-N-(methylsulfonyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 4-Hexadecylaminobenzoyl chloride hydrochloride | HCID 13255322 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | p-Hexadecylamino-N-(methylsulfonyl)benzamide | HCID 20437358 | — |
Reaction Steps
A solution of 25.2 g. of 4-(hexadecylamino)benzoyl chloride hydrochloride and 5.8 g. of methanesulfonamide in 250 ml. of pyridine was stirred under reflux for 2 hours and then concentrated in vacuo. The residue was partitioned between water and diethyl ether; the aqueous layer acidified with 1 N HCl, and the organic layer separated, dried (MgSO4), and evaporated. Crystallization of the residual white solid from 60% aqueous acetic acid followed by CH2Cl2 -hexane afforded the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242273 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-015213ca0d38459f99b003e330aa906e |
| Source note | uspto-grants-1980_12 |