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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671283Generated: November 1, 2026

Benzaldehyde → 2-Chloro-α-phenyl-6-(trifluoromethyl)-3-pyridinemethanol

https://huagongshe.com/reaction/1671283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantWaterHCID 962—
Reactant2-Chloro-6-(trifluoromethyl)pyridineHCID 602334—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-α-phenyl-6-(trifluoromethyl)-3-pyridinemethanolHCID 8663876199.7%

Reaction Steps

Lithium diisopropylamide (3.7 mL, 1.8 M tetrahydrofuran solution, manufactured by Tokyo Chemical Industry Co., Ltd.) was added to a solution of 2-chloro-6-(trifluoromethyl)pyridine (1.0 g, manufactured by Matrix Chemical LLC) in tetrahydrofuran (55 mL, manufactured by Kanto Chemical Co., Inc.) at −78° C., and the mixture was stirred for 30 minutes at the same temperature. Then, benzaldehyde (1.17 g, manufactured by Kokusan Chemical Co., Ltd.) was added thereto at −78° C., and the mixture was stirred overnight while gradually raising the temperature to room temperature. Water (50 mL) was added to the reaction solution, and the mixture was extracted with ethyl acetate (3×10 mL), washed with brine (20 mL), and dried (MgSO4). The solvent was then evaporated. The resulting residue was purified by silica gel column chromatography (chloroform:methanol=9:1), to give 1.58 g of the title compound. LC-MS: HPLC retention time 1.68 minutes, m/z 288 (M+H), condition C-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994202B2
Source datasetuspto-grants-2011_08
ORD IDord-6a5aa57d5efb4eb8a8cf4a9d91faa776
Source noteuspto-grants-2011_08