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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100677Generated: October 31, 2026

tert-Butyl acrylate → 3-{4-[4-(4-Chloro-3-trifluoromethyl-benzyloxy)-phenyl]-piperidin-1-yl}-propionic acid tert-butyl ester

https://huagongshe.com/reaction/2100677

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acrylateHCID 15458—
Reactant4-[4-(4-Chloro-3-trifluoromethyl-benzyloxy)-phenyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 68813008—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product3-{4-[4-(4-Chloro-3-trifluoromethyl-benzyloxy)-phenyl]-piperidin-1-yl}-propionic acid tert-butyl esterHCID 68813022—

Reaction Conditions

Temperature90 °C

Reaction Steps

4-[4-(4-Chloro-3-trifluoromethyl-benzyloxy)-phenyl]-piperidine-1-carboxylic acid tert-butyl ester (1 eq) is dissolved in 10% TFA/DCM and stirred for 30 minutes. After concentration, the residue is re-dissolved in DCM and washed with saturated NaHCO3 and brine. The organic layer is dried over Na2SO4 and concentrated. The residue is then dissolved in MeOH and t-butyl acrylate (2 eq) is added. The resulting solution is heated at 90° C. in microwave for 10 minutes. After concentration, purification by flash column chromatography (80% EtOAc/hexane) gave 3-{4-[4-(4-Chloro-3-trifluoromethyl-benzyloxy)-phenyl]-piperidin-1-yl}-propionic acid tert-butyl ester. [MS: (ES+) 498.2 (M+1)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572811B2
Source datasetuspto-grants-2009_08
ORD IDord-ea4827422dd7499eb8814aa11b10c838
Source noteuspto-grants-2009_08