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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220048Generated: October 29, 2026

Potassium tert-butoxide → 1-Acetyl-5-[4-(2,2-difluoroethyl)phenyl]piperidine-3-carboxylic acid

https://huagongshe.com/reaction/220048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMethyl 1-acetyl-5-[4-(2,2-difluoroethyl)phenyl]piperidine-3-carboxylateHCID 59606565—
SolventMethanolHCID 887—
Product1-Acetyl-5-[4-(2,2-difluoroethyl)phenyl]piperidine-3-carboxylic acidHCID 59606579—

Reaction Conditions

Temperature60 °C

Reaction Steps

410 mg (3.65 mmol) of potassium tert-butoxide were added at RT to a solution of 205 mg (0.365 mmol, purity 61%) of the compound from Example 58A in methanol (6.9 ml). The mixture was stirred at 60° C. overnight. For workup, the methanol was removed under reduced pressure, the residue was admixed with water and the mixture was acidified (pH 1) with aqueous 1 N hydrochloric acid solution. The mixture was extracted with ethyl acetate, and the organic phase was dried with magnesium sulphate, filtered and concentrated under reduced pressure. Yield: 153 mg (67% of theory, purity 50%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202862B2
Source datasetuspto-grants-2012_06
ORD IDord-f02235104ddc49259f89ec76b46f8cb5
Source noteuspto-grants-2012_06