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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4742Generated: October 26, 2026

Sulfuric Acid → alpha,alpha-Bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene

https://huagongshe.com/reaction/4742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(p-Tolyl)hexafluoroisopropanolHCID 74829—
Catalystchromium (VI) trioxideHCID 10219390—
SolventWaterHCID 962—
Productalpha,alpha-Bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]tolueneHCID 14076668—

Reaction Steps

To a solution of 156 g (0.60 mole) of 4-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]toluene in 675 ml of acetic anhydride is added 135 ml of concentrated sulfuric acid at 0°. To the solution stirred at 0° is added a soluton of 168 g (1.68 mole) of chromium trioxide in 750 ml of acetic anhydride dropwise over a two-hour period. After stirring is continued for an additional two hours, the resulting reaction mixture is poured into five liters of ice and is diluted with five liters of water to obtain an aqueous mixture which is allowed to stand for 18 hours. An oily solid with water above it is obtained. Water is decanted from the oily solid. The solid is dissolved in ether to obtain a solution which is washed with water and sodium bicarbonate solution, dried with anhydrous magnesium sulfate, filtered and evaporated at reduced pressure to give an oily solid. The solid is triturated with ether, filtered and recrystallized from chlorobutane to give 60 g of α,α -bis-acetyloxy-4-[1-(acetyloxy)-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]toluene, m.p. 93°-94.6°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04727180
Source datasetuspto-grants-1988_02
ORD IDord-444e854447fe4b53ac481a298adcab6e
Source noteuspto-grants-1988_02