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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413941Generated: November 4, 2026

Hexafluoroacetone → 1,1,1,3,3,3-Hexafluoro-2-(1,2,3,4-tetrahydroquinolin-6-yl)propan-2-ol

https://huagongshe.com/reaction/1413941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexafluoroacetoneHCID 12695—
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
CatalystAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
Product1,1,1,3,3,3-Hexafluoro-2-(1,2,3,4-tetrahydroquinolin-6-yl)propan-2-olHCID 1362653369.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

Two hundred grams of 1,2,3,4-tetrahydroquinoline and 2 g anhydrous aluminum chloride are added to a one liter stainless steel reactor. The reactor is cooled and evacuated, 265 g (1.60 moles) hexafluoroacetone is added, and it is sealed and heated to 120° C. with shaking for ten hours. The reactor is then cooled to room temperature and vented. The contents are decanted to give a red semicrystalline solid, which is treated with 250 ml of methylene chloride and filtered. The filter cake is washed with three additional 250 ml portions of methylene chloride. The residual orange solid is treated with decolorizing carbon in hot chlorobutane and filtered. From the filtrate is obtained 310 g (1.04 moles) α,α-bis(trifluoromethyl)-1,2,3,4-tetrahydro-6-quinolinemethanol, as a pale yellow crystalline solid, m.p. 115°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04251659
Source datasetuspto-grants-1981_02
ORD IDord-3ed6fd0e850748c598e15442cf6d5d92
Source noteuspto-grants-1981_02