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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647706Generated: October 31, 2026

Pyridine → N-benzyl-N-methyl-2(S)-(3,4-dichlorophenyl)-4-pentenoamide

https://huagongshe.com/reaction/1647706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantN-MethylbenzylamineHCID 7669—
ReactantOxalyl chlorideHCID 65578—
Reactant(S)-2-(3,4-dichlorophenyl)pent-4-enoic acidHCID 15261879—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-benzyl-N-methyl-2(S)-(3,4-dichlorophenyl)-4-pentenoamideHCID 15288290—

Reaction Steps

A solution of 4.8 g (19.6 mmol) of 2-(S)-(3,4-dichlorophenyl)-4-pentenoic acid in 50 mL of CH2Cl2 and 10 drops of DMF was cooled in an ice bath and 1.8 mL of oxalyl chloride was added. The solution was stirred for 15 min after gas evolution had ceased. The mixture was concentrated in vacuo and the residue was diluted with 50 mL of CH2Cl2. The solution was cooled in ice bath as 2.6 mL (20.4 mmol) of N-benzyl-methyl amine and 1.7 mL (21 mmol) of pyridine were added. After stirring for 1 h at ice bath temperature the solution was diluted with CH2Cl2 and washed with water, 1.2N HCl and brine. The solution was dried over Na2SO4 and concentrated to give N-benzyl-N-methyl-2(S)-(3,4-dichlorophenyl)-4-pentenoamide as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434158
Source datasetuspto-grants-1995_07
ORD IDord-ee4b5f70583b49ca9a142d52169ab810
Source noteuspto-grants-1995_07