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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659079Generated: October 29, 2026

Chloroacetyl chloride → N-(1-Benzyl-piperidin-4-yl)-2-chloro-N-isopropyl-acetamide

https://huagongshe.com/reaction/659079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Benzyl-N-isopropylpiperidin-4-amineHCID 10728310—
SolventDichloromethaneHCID 6344—
ProductN-(1-Benzyl-piperidin-4-yl)-2-chloro-N-isopropyl-acetamideHCID 6656516550.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 1-benzyl-4-(isopropylamino)piperidine (8 g, 34.45 mmol) and DIPEA (7.2 mL, 41.3 mmol) in 200 mL of dichloromethane was added dropwise a solution of 2-chloroacetyl chloride (3.01 mL, 37.9 mmol) in dichloromethane (400 mL) at 0° C. The reaction mixture was stirred at 0° C. for 15 min and then at room temperature for 2 h. The reaction mixture was then washed with saturated sodium bicarbonate, brine, dried over magnesium sulfate and concentrated in vacuo. The resulting residue was purified by flash column chromatography (ethyl acetate/hexane/triethylamine: 42.5/56.5/1) to give 5.35 g of the title intermediate as a viscous oil (50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08080565B2
Source datasetuspto-grants-2011_12
ORD IDord-64ceaa9e27b34369b9ec8a7b788eef19
Source noteuspto-grants-2011_12