HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888335Generated: October 30, 2026
Hydrochloric Acid → HCID 59378486, compound
https://huagongshe.com/reaction/888335
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 | HCID 59378472 | HCID 59378472 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 59378486 | HCID 59378486 | 37.7% |
Reaction Steps
To a solution of 0.7 g of 3-ethyl-5-hexynyl methanesulfonate and 0.7 g of (3,3,3-trifluoropropylsulfonyl)acetonitrile in 20 ml of dimethyl sulfoxide was added 0.5 g of potassium carbonate at room temperature. The reaction mixture was stirred at 60° C. for 20 hours. 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 0.40 g of 5-ethyl-2-(3,3,3-trifluoropropylsulfonyl)-7-octynenitrile (hereinafter referred to as the present compound (29)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247595B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-35a1caaa43604e7986deb07ee7454bb9 |
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| Source note | uspto-grants-2012_08 |
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