Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541214Generated: October 26, 2026

Methanol → Methyl 5-(4-(4-cyanophenyl)piperidine-1-carbonyl)-2-methylbenzoate

https://huagongshe.com/reaction/541214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant5-(4-(4-Cyanophenyl)piperidine-1-carbonyl)-2-methylbenzoic acidHCID 68288381—
ProductMethyl 5-(4-(4-cyanophenyl)piperidine-1-carbonyl)-2-methylbenzoateHCID 6828906190%

Reaction Steps

To a stiffed mixture of 5-(4-(4-cyanophenyl)piperidine-1-carbonyl)-2-methylbenzoic acid (compound 39.3, 1.392 g, 4.00 mmol, 1.00 equiv) in methanol (50 mL) was added sulfuric acid (784 mg, 7.99 mmol, 2.00 equiv), dropwise. The resulting mixture was heated to reflux overnight in an oil bath. After cooling to ambient temperature, the organic solvent was removed under reduced pressure. The residue was diluted with 20 mL of EtOAc and was washed with 1×100 mL of saturated sodium bicarbonate(aq) followed by 1×100 mL of brine. The organic layer was dried (Na2SO4) and concentrated under reduced pressure to yield 1.303 g (90%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-428f99b90a60475aae5aed1fc4c48d08
Source noteuspto-grants-2014_10