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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620602Generated: November 5, 2026

Water → 1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carboxylic acid

https://huagongshe.com/reaction/1620602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2,4-Bis(trifluoromethyl)benzyl bromideHCID 518871—
Reactant2-Oxopiperidine-4-carboxylic acidHCID 55286080—
SolventTetrahydrofuranHCID 8028—
Product1-[2,4-Bis(trifluoromethyl)benzyl]-2-oxopiperidine-4-carboxylic acidHCID 8667877358.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-oxopiperidine-4-carboxylic acid (21.3 g) in tetrahydrofuran (300 mL) was added 60% sodium hydride (18 g, containing mineral oil) under cooling to 0° C. The reaction mixture was stirred for 30 min under cooling to 0° C. To the reaction mixture was added dropwise 1-(bromomethyl)-2,4-bis(trifluoromethyl)benzene (46 g) under cooling to 0° C., and the mixture was further stirred at 80° C. for 2 days. Water was added to the reaction mixture under cooling to 0° C., and the mixture was extracted with ethyl acetate. To the aqueous layer was further added 10% hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (32 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-6f0cb7cf409f4b6da26145a8fe848f96
Source noteuspto-grants-2014_07