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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1905824Generated: November 3, 2026

Methane → 1,1,1,3,3,3-Hexafluoro-2-propanol

https://huagongshe.com/reaction/1905824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantHexafluoroacetoneHCID 12695—
CatalystPalladiumHCID 23938—
Product1,1,1,3,3,3-Hexafluoro-2-propanolHCID 13529—

Reaction Steps

French Pat. No. 2,027,172 relates to a process for gas phase hydrogenation of perhaloketones over a palladium-based catalyst deposited on activated charcoal and particularly describes catalytic hydrogenation of hexafluoroacetone (CF3COCF3) to yield 1,1,1,3,3,3-hexafluoroisopropyl alcohol. The yield obtained (75%) and the difficulty of handling the starting material (b.p.: -27.4° C./760 torr) make the process uneconomical. French Pat. No. 2,479,803 carries out a gas phase catalytic hydrogenation of hexafluoroacetone to 1,1,1,3,3,3-hexafluoroisopropanol over a nickel-based catalyst. The catalyst life is not rated for a continuous operation time longer than 20 hours and, above all, this process requires the use of a pure starting material, which is difficult to obtain in the case of hexafluoroacetone. French Pat. No. 1,361,260 carries out the gas phase catalytic hydrogenation of hexafluoroacetone over a catalyst based on copper chromite. The yields of 1,1,1,3,3,3-hexafluoroisopropanol are mediocre (approximately 40%) for a partial conversion (83%) of the ketone used. This entails difficult and costly recycling.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04647706
Source datasetuspto-grants-1987_03
ORD IDord-5beb760d57d34c4d81b44b6f448e180f
Source noteuspto-grants-1987_03