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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717304Generated: October 31, 2026

Toluene → (4-Benzyl-4-hydroxypiperidin-1-yl)(2-chloropyridin-3-yl)methanone

https://huagongshe.com/reaction/717304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantThionyl ChlorideHCID 24386—
Reactant2-Chloronicotinic acidHCID 76258—
Product(4-Benzyl-4-hydroxypiperidin-1-yl)(2-chloropyridin-3-yl)methanoneHCID 86680867—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 2-chloronicotinic acid (1.0 g), toluene (15 mL) and DME (5 mL) was added thionyl chloride (0.51 mL), and the mixture was stirred at 90° C. for 4 hr under a nitrogen atmosphere. The reaction mixture was concentrated under reduced pressure, the residue was dissolved in THF (15 mL), and triethylamine (0.97 mL) and 4-benzyl-4-hydroxypiperidine (1.1 g) were added thereto. The reaction mixture was stirred overnight at room temperature under a nitrogen atmosphere, saturated aqueous sodium hydrogen carbonate solution was added thereto, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193709B2
Source datasetuspto-grants-2015_11
ORD IDord-14c138e7aafd44b9be3676424e9cab1f
Source noteuspto-grants-2015_11