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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1452695Generated: October 31, 2026

Trifluoroacetic acid methylene chloride → HCID 11710738, compound

https://huagongshe.com/reaction/1452695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acid methylene chlorideHCID 21863450—
ReactantHCID 86604223HCID 86604223—
ProductHCID 11710738HCID 1171073812%

Reaction Steps

82 mg (0.2 mmol) of crude 1-benzyloxy-2-chloro-4-[2,2,2-trifluoro-1-(4-methoxy-benzyloxy)-1-trifluoromethyl-ethyl]-benzene were treated with 3 mL of a mixture of dichloromethane/trifluoroacetic acid (1:3) at room temperature for 1 h. The solvent was evaporated and the residue was redissolved in a mixture of diethyl ether and a solution of Na2CO3. The inorganic phase was extracted with diethyl ether and the combined organic phases were washed with brine and dried (Na2SO4). After filtration and evaporation of the solvent, the crude product was purified by column chromatography to give 7.3 mg (12%) of 2-(4-benzyloxy-3-chloro-phenyl)-1,1,1,3,3,3-hexafluoro-propan-2-ol as a yellow gum, MS: 383 (M−H, 1Cl)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07473705B2
Source datasetuspto-grants-2009_01
ORD IDord-65c26d97a48b46168ff4fd7c3b28ac17
Source noteuspto-grants-2009_01