HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268075Generated: November 1, 2026
Triethylamine → 1-Methanesulfonyloxy-7,7,8,8,8-pentafluorooctane
https://huagongshe.com/reaction/1268075
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 7,7,8,8,8-Pentafluorooctan-1-ol | HCID 2775949 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Methanesulfonyloxy-7,7,8,8,8-pentafluorooctane | HCID 18544009 | 89% |
Reaction Steps
7,7,8,8,8-Pentafluorooctan-1-ol(25 g, 113 mmol) was dissolved in dichloromethane (250 ml), triethylamine(47.4 ml, 339 mmol) and methanesulfonylchloride(17.6 ml, 227 mmol) were added dropwise under cooling to 0° C., and the resulting mixture was stirred for 1 hour. The reaction solution was diluted with water, extracted twice with dichloromethane(200 ml), washed with water and saturated saline solution, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (eluent:ethyl acetate/n-hexane=1/10, v/v) to give 30 g(100 mmol, Yield 89%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06555571B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-c7ed5dd5fb604b54a3dc17b1c1632a80 |
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| Source note | uspto-grants-2003_04 |
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