HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[(Methylsulfonyl)oxy]-5-hexynenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-Hydroxy-5-hexynenitrile | HCID 13044948 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[(Methylsulfonyl)oxy]-5-hexynenitrile | HCID 13044949 | 87.4% |
Reaction Steps
A mixture of 2-hydroxy-5-hexynenitrile (8.0 g, 73.3 mmol) and dry triethylamine (10.1 g, 0.1 mol) in 50 ml of dry CH2Cl2 was treated with a solution of methanesulfonyl chloride (10.3 g, 90 mmol) in 50 ml of CH2Cl2, at 0° C. for 11/2 h. The reaction mixture was diluted with CH2Cl2, washed twice with cold 1.0 N H2SO4, twice with water, and dried over MgSO4. The filtered CH2Cl2 solution was concentrated at 40° C./30 mm to give 12 g of pale yellow liquid. Purification of this material on 220 g of silica gel and eluted with ether-petroleum ether (1:1 parts by volume) gave 8.7 g (56% by weight yield from pentynal) of 2-[(methylsulfonyl)]-5-hexynenitrile as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04345084 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-f13fcae9cc194a85bc352a03ac6af345 |
| Source note | uspto-grants-1982_08 |