HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888334Generated: October 25, 2026
Hydrochloric Acid → 6-Methyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrile
https://huagongshe.com/reaction/888334
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(3,3,3-Trifluoropropylsulfonyl)acetonitrile | HCID 57425671 | — |
| Reactant | 4-Methyl-5-hexynyl methanesulfonate | HCID 59378474 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-Methyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrile | HCID 86642987 | 29% |
Reaction Steps
To a solution of 1.0 g of 4-methyl-5-hexynyl methanesulfonate and 1.1 g of (3,3,3-trifluoropropylsulfonyl)acetonitrile in 30 ml of dimethyl sulfoxide was added 0.7 g of potassium carbonate at room temperature. The reaction mixture was stirred at 60° C. for 2 days. The reaction mixture was allowed to stand to cool to nearly room temperature. To the reaction mixture was added 10% hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The obtained residue was subjected to silica gel chromatography to obtain 0.45 g of 6-methyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrile (hereinafter referred to as the present compound (28)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08247595B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-15d67979df5441e292fb499fbfecbcaf |
|---|
| Source note | uspto-grants-2012_08 |
|---|