HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 4-(2-Tetrahydropyranyloxy)nonylamine | HCID 20327684 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamide | HCID 20327650 | — |
Reaction Steps
To a stirred, ice cold solution of 4-(2-tetrahydropyranyloxy)nonylamine (7.29 g., 0.03 mole) in pyridine (40 ml.) is added methanesulfonylchloride (3.42 g., 0.03 mole) at such a rate as to maintain the reaction temperature at 5°-10° C. The reaction is then allowed to stand at room temperature for six hours, poured into ice water (200 ml.) and extracted with ether (2× 100 ml.). The ether is washed with ice cold 5% hydrochloric acid (2× 20 ml.), with brine (2× 25 ml.), and then dried over sodium sulfate. Evaporation in vacuo affords N-[4-(2-tetrahydropyranyloxy)nonyl]methanesulfonamide as a pale yellow liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04033996 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-41000eec5377490698155d880af27729 |
| Source note | uspto-grants-1977_07 |