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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350281Generated: October 31, 2026

Trifluoroacetic acid → HCID 59909762, compound

https://huagongshe.com/reaction/1350281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59909851HCID 59909851—
SolventDichloromethaneHCID 6344—
ProductHCID 59909762HCID 5990976299.7%

Reaction Steps

A solution of methyl 2-{(1R)-1-[2-(tert-butoxy)-2-oxoethyl]-4-cyclohexylbutyl}-5-methyl-1,3-oxazole-4-carboxylate (Preparation 173) (2.92 g, 7.43 mmol) in anhydrous dichloromethane (15 ml) was treated with trifluoroacetic acid (7.5 ml) and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 24 hours. The solvent was removed under reduced pressure and the residue was azeotroped with dichloromethane (×3). The residue was purified by column chromatography on silica gel eluting with a gradient system of ethyl acetate:pentane (0:100 to 40:60) to afford the title compound as a colourless oil (2.50 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214694B2
Source datasetuspto-grants-2007_05
ORD IDord-2396081cf31b466db58a9c878224be4a
Source noteuspto-grants-2007_05