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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588058Generated: November 2, 2026

Water → HCID 71495336, compound

https://huagongshe.com/reaction/588058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzylpiperidin-4-olHCID 78461—
ReactantHCID 1419048HCID 1419048—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
ProductHCID 71495336HCID 7149533659.3%

Reaction Steps

A solution of 1-benzyl-4-hydroxypiperidine (209 mg, 1.1 mmol, 1.1 eq) and 95 w % sodium hydride (1.2 mmol) in 5 ml of dimethylformamide was stirred at a room temperature for 30 min, mixed with 2-chloro-N-(3-chlorophenyl)nicotinamide (1.0 mmol), and stirred for 20 hrs under reflux. The reaction mixture was cooled to a room temperature, and added with 20 ml of pure water to terminate the reaction. After two rounds of extraction with 20 ml of ethylacetate per round, water was removed with a desiccant and the resulting product was concentrated under reduced pressure. Then, the residue obtained by the concentration was subjected to silica gel column chromatography (mobile phase: 30 (v/v) % hexane in EA) to obtain the desired fraction. The desired fraction was dried in a reduced pressure to afford 0.25 g of the title compound (Yield: 33.7%). 1H NMR (CDCl3) δ 8.60 (d, 1H), 8.29 (d, 1H), 7.88 (s, 1H), 7.48 (d, 1H), 7.36-7.27 (m, 6H), 7.17-7.05 (m, 2H), 5.51-5.38 (m, 1H), 3.59 (s, 2H), 2.89-2.80 (m, 2H), 2.42 (t, 2H), 2.29-2.23 (m, 2H), 2.06-1.87 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227955B2
Source datasetuspto-grants-2016_01
ORD IDord-136f88f3507d46f9a79de804233734b4
Source noteuspto-grants-2016_01