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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989782Generated: October 29, 2026

Dichloromethane → N-piperidinopropyl-5-(3,4-dichlorophenyl)-3-methyl-pentadiene carboxamide

https://huagongshe.com/reaction/989782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
ReactantPiperidino-propylamineHCID 18419402—
Reactant5-(3,4-dichlorophenyl)-3-methyl-pentadienoic AcidHCID 85811893—
ProductN-piperidinopropyl-5-(3,4-dichlorophenyl)-3-methyl-pentadiene carboxamideHCID 88175739—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 5-(3,4-dichlorophenyl)-3-methyl-pentadienoic acid (0.100 g, 0.390 mmol) in CH2Cl2 (5 mL) is treated with triethyl-amine (0.050 cr, 0.050 mmol) and cooled to 0° C. The resulting colorless solution is then treated with isobutyl chloroformate (0.065 g, 0.050 mmol). After 30 min., piperidino-propylamine (0.071 g, 0.050 mmol) is added, and the reaction mixture is allowed to warm to room temperature. After stirring overnight, the reaction mixture is quenched with aqueous sodium bicarbonate. The aqueous layer is extracted several times with CH2Cl2, and the combined organic layers are dried (sodium sulfate), and concentrated in vacuo. The residue is treated with excess methanolic HCl, evaporated in vacuo, and rinsed with ether to yield 0.159 g of a hygroscopic white solid, mp 50-60° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458806B1
Source datasetuspto-grants-2002_10
ORD IDord-b67944bef1b641c29bb85de48b76ef73
Source noteuspto-grants-2002_10