HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-chloro-N-(2,2,3,3,4,4,4-heptafluorobutyl)-N-methyl-pentanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 12589202 | HCID 12589202 | — |
| Reactant | N-(2,2,3,3,4,4,4-heptafluorobutyl)-N-methylamine hydrochloride | HCID 19711030 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-chloro-N-(2,2,3,3,4,4,4-heptafluorobutyl)-N-methyl-pentanesulfonamide | HCID 19711032 | 101.5% |
Reaction Steps
500 mg of N-(2,2,3,3,4,4,4-heptafluorobutyl)-N-methylamine hydrochloride (obtained according to European Patent No. 384,842 Example 75) and then, at 0° to 5° C., 0.55 ml of triethylamine were added to a solution of 200 mg of 5-chloropentane sulfonyl chloride in 5 ml of methylene chloride, and the mixture was stirred at ambient temperature for 2 hours. Water was added and extraction was carried out with methylene chloride. The extracts were washed with water, then with a saturated aqueous solution of sodium chloride, dried and evaporated to dryness under reduced pressure to obtain 378 mg of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05556845 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-cc4a513edc624cf086f8940b14efdc17 |
| Source note | uspto-grants-1996_09 |