HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Methylsulfonyloxy-5-(2-propenyl)-hexanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 14986704 | HCID 14986704 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Methylsulfonyloxy-5-(2-propenyl)-hexanenitrile | HCID 14986705 | — |
Reaction Steps
To a solution of 2679 g of 6-hydroxy-5-(2-propenyl)-hexanenitrile in 25 l of methylene chloride is added 2681 ml of triethylamine. The mixture is cooled to -10° in an ice salt bath and a solution of 2103 g of methanesulfonyl chloride in 2 l of methylene chloride is added dropwise over 3 h keeping the temperature at -5°. After addition is complete, the mixture is stirred for 3 h in an ice salt bath and then overnight at 10°. The mixture is washed with water, saturated sodium bicarbonate solution, water and then brine, dried over sodium sulfate, evaporated to dryness, and dried at 45°/3 mm Hg (=4.00 mbar) to yield 6-methylsulfonyloxy-5-(2-propenyl)-hexanenitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153214 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-12297be2b1cb402aa291ef1e879fa851 |
| Source note | uspto-grants-1992_10 |