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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654217Generated: November 3, 2026

Trifluoroacetic acid → HCID 22852538, compound

https://huagongshe.com/reaction/1654217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 22852539HCID 22852539—
SolventEthanolHCID 702—
ProductHCID 22852538HCID 22852538131.4%

Reaction Steps

In ethanol (8.5 ml) was dissolved (3R)-2-(2,4-difluorophenyl)-1-(1-imidazolyl)-3-(3,4,5,6-tetrahydro-2H-pyran-2-yloxy)-2-butanol (1.7 g) followed by addition of trifluoroacetic acid (8.5 ml) at 0° C. After 10 minutes, the temperature was adjusted to 20° C. and the mixture was allowed to stand for 1 hour. The reaction mixture was then concentrated under reduced pressure and the residue was subjected to silica gel chromatography (2 cm×10 cm) using methanol-methylene chloride (1:9) as the eluent. The desired fraction was concentrated to give (3R)-2-(2,4-difluorophenyl)-1-(1-imidazolyl)-2,3-butanediol (1.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05405861
Source datasetuspto-grants-1995_04
ORD IDord-6fa958e075f34af2b87ca3d70ae2c6a1
Source noteuspto-grants-1995_04