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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1726127Generated: November 3, 2026

1-Bromo-4-(trifluoromethoxy)benzene → 1-Boc-4-[Hydroxy-(4-trifluoromethoxyphenyl)methyl]piperidine

https://huagongshe.com/reaction/1726127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-(trifluoromethoxy)benzeneHCID 521008—
Reactanttert-Butyl 4-formylpiperidine-1-carboxylateHCID 1514430—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1-Boc-4-[Hydroxy-(4-trifluoromethoxyphenyl)methyl]piperidineHCID 1205278466.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1-bromo-4-(trifluoromethoxy)benzene (1.88 g, 7.80 mmol) in THF (16 mL) at −78° C. was added n-BuLi (1.9M in hexanes, 4.1 mL, 7.8 mmol), and the solution was stirred at −78° C. for 30 minutes. A solution of 4-formyl-piperidine-1-carboxylic acid tert-butyl ester (1.50 g, 7.03 mmol) in THF (2 mL) was added dropwise, and the mixture was stirred at −78° C. for 45 minutes then allowed to warm to room temperature over 1 h. Work-up and purification gave 4-[hydroxy-(4-trifluoromethoxy-phenyl)-methyl]-piperidine-1-carboxylic acid tert-butyl ester as colourless crystals (1.75 g, 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491735B2
Source datasetuspto-grants-2009_02
ORD IDord-e7a88e6e918f4f039f054724f682ebce
Source noteuspto-grants-2009_02