HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240409Generated: October 29, 2026
Toluene → (4-Benzyl-4-hydroxypiperidin-1-yl)(2-chloropyridin-3-yl)methanone
https://huagongshe.com/reaction/240409
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Chloronicotinic acid | HCID 76258 | — |
| Product | (4-Benzyl-4-hydroxypiperidin-1-yl)(2-chloropyridin-3-yl)methanone | HCID 86680867 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648079B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-e5f7df74cd774363895ee528046cda90 |
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| Source note | uspto-grants-2014_02 |
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