Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726241Generated: November 2, 2026

1-Boc-4-[Hydroxy-(4-trifluoromethoxyphenyl)methyl]piperidine → tert-Butyl 4-(4-(trifluoromethoxy)benzoyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1726241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Boc-4-[Hydroxy-(4-trifluoromethoxyphenyl)methyl]piperidineHCID 12052784—
ReactantHCID 178418287HCID 178418287—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-(4-(trifluoromethoxy)benzoyl)piperidine-1-carboxylateHCID 68968884100%

Reaction Steps

To a solution of 4-[hydroxy-(4-trifluoromethoxy-phenyl)-methyl]-piperidine-1-carboxylic acid tert-butyl ester (see EXAMPLE 32) (604 mg, 1.61 mmol) in CH2Cl2 (8 mL) was added SiO2 (2 g) followed by PCC (1.04 g, 4.82 mmol), and the mixture was stirred at room temperature for 3 h to give 4-(4-trifluoromethoxy-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester as colourless crystals (601 mg, 100%) after purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-aa4a1224a10c4668b12cbc71c6360b25
Source noteuspto-grants-2009_02