HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → N-[4-[14-(Trimethylsilyl)tetradecylamino]benzoyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | 4-[14-(Trimethylsilyl)tetradecylamino]benzoyl chloride hydrochloride | HCID 20198230 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[4-[14-(Trimethylsilyl)tetradecylamino]benzoyl]methanesulfonamide | HCID 20198291 | — |
Reaction Steps
A solution of 12.3 g. of 4-[14-(trimethylsilyl)tetradecylamino]benzoyl chloride hydrochloride and 2.8 g. of methanesulfonamide in 150 ml. of pyridine is stirred at reflux for 2 hours and then evaporated in vacuo. The residue is partitioned between water and diethyl ether, the aqueous layer acidified with 1N hydrochloric acid, and the organic layer separated, dried with magnesium sulfate and evaporated. Crystallization of the residue affords the product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04670421 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-ae62468ef3c546e7b5459000a2be9856 |
| Source note | uspto-grants-1987_06 |