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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591619Generated: October 31, 2026

Benzoyl chloride → Ethyl 4-(4-benzamidopiperidin-1-yl)benzoate

https://huagongshe.com/reaction/591619

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
ReactantEthyl 4-(4-aminopiperidin-1-yl)benzoateHCID 22557718—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-(4-benzamidopiperidin-1-yl)benzoateHCID 66670912100%

Reaction Steps

To a solution of ethyl 4-(4-aminopiperidin-1-yl)benzoate (3.0 g, 12.1 mmol) in CH2Cl2 under nitrogen was added Et3N (2.45 g, 24.2 mmol), followed by benzoyl chloride (1.70 g, 12.1 mmol). The mixture was stirred at room temperature overnight, washed with brine (200 mL), dried over anhydrous MgSO4, filtered, and concentrated. The resulting solids were triturated with hexanes to afford ethyl 4-(4-benzamidopiperidin-1-yl)benzoate as a yellow solid (4.2 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238640B2
Source datasetuspto-grants-2016_01
ORD IDord-3dc5a8ba799540dcbebc3efd0229f58f
Source noteuspto-grants-2016_01