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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1979916Generated: October 26, 2026

Acetic Acid → 2-Bromomethyl-decafluoropentan-2-ol

https://huagongshe.com/reaction/1979916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPerfluoropropyl iodideHCID 33977—
Reactant3-Bromo-1,1,1-trifluoro-2-propanoneHCID 79008—
ReactantHCID 178418255HCID 178418255—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-Bromomethyl-decafluoropentan-2-olHCID 5382619782%

Reaction Conditions

Temperature-20 °C

Reaction Steps

Heptafluoropropyl iodide (5 g, 16.9 mmole) was stirred in dry diethyl ether (20 ml) at -78° C. Phenylmagnesium bromide (10 ml of a 1.88M solution in ether) was then added dropwise, keeping the temperature below -65° C. When the addition was complete, the reaction mixture was stirred at -20° C. for one hour. It was then cooled to -78° C. and 3-bromo-1,1,1-trifluoropropanone (4.87 g, 18.0 mmole) in dry diethylether (20 ml) was added dropwise, keeping the temperature below -65° C. When the addition was complete, the mixture was stirred at between -20° and -50° C. for four hours. Glacial acetic acid (3 ml) in diethyl ether (5 ml) was then added slowly, followed by water (15 ml). The mixture was then allowed to warm to 5° C. and the phases were separated. The aqueous phase was washed with ether (2×25 ml). The ethereal extracts were combined, dried (MgSO4) and evaporated to give crude 2-bromomethyl-decafluoropentan-2-ol (5.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04483862
Source datasetuspto-grants-1984_11
ORD IDord-ee42249280ba4c588ba02f30508324a1
Source noteuspto-grants-1984_11