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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250524Generated: November 3, 2026

4-Methylbenzoyl Chloride → HCID 20718668, compound

https://huagongshe.com/reaction/1250524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methylbenzoyl ChlorideHCID 13405—
ReactantHCID 18346053HCID 18346053—
SolventPyridineHCID 1049—
ProductHCID 20718668HCID 2071866855.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

p-Toluoyl chloride (0.14 ml, 1 mmol) was added to a solution of 1-(S)-[4-(3,4-dichlorobenzyl)piperidin-1-ylmethyl]-2-methylpropylamine (0.33 g, 1 mmol) in dry pyridine (7 ml) at 0° C. under argon atmosphere. The solution was stirred for 30 min., at 0° C. and then allowed to warm to room temperature. After 3 h, the reaction mixture was concentrated under reduced pressure and water (10 ml) was added. The product was extracted with ethyl acetate and the organic layer was dried with magnesium sulfate and then concentrated in vacuo. The crude product (0.5 g) was chromatographed by eluting with a gradient of from 1% to 4% methanol/methylene chloride to give N-{1-(S)-[4-(3,4-dichlorobenzyl)piperidin-1-ylmethyl]-2-methylpropyl}-4-methylbenzamide (0.25 g) as partially solidified gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339087B1
Source datasetuspto-grants-2002_01
ORD IDord-1047bb6b281e4768b9228f4de07c0caa
Source noteuspto-grants-2002_01