HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888329Generated: October 31, 2026
Hydrochloric Acid → HCID 86642983, compound
https://huagongshe.com/reaction/888329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Bromo-1-hexene | HCID 75906 | — |
| Reactant | Methyl 2-(3,3,3-trifluoropropylsulfonyl)acetate | HCID 57425720 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 86642983 | HCID 86642983 | 79.9% |
Reaction Steps
To a solution of 2.0 g of 6-bromo-1-hexene and 2.9 g of methyl (3,3,3-trifluoropropylsulfonyl)acetate in 50 ml of dimethyl sulfoxide, 0.5 g of sodium hydride (60% in oil) was added at room temperature. The mixture was heated to 60° C., stirred for 4 hours, and then allowed to stand near room temperature. To the reaction mixture, 10% hydrochloric acid was added, followed by extraction 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 3.10 g of methyl 2-(3,3,3-trifluoropropylsulfonyl)-7-octenoate (hereinafter referred to as the present compound (20)).
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-4ce8cad8df7040efb66302c0450b9e6b |
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| Source note | uspto-grants-2012_08 |
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