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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846668Generated: November 3, 2026

Benzoyl chloride, 3-chloro- → HCID 68304434, compound

https://huagongshe.com/reaction/1846668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chloride, 3-chloro-HCID 69252—
ReactantHCID 67323853HCID 67323853—
SolventAcetonitrileHCID 6342—
ProductHCID 68304434HCID 6830443456.7%

Reaction Steps

To a solution of 0.710 g (2.39 mmol) of [1-(2-amino-4-chloro-phenyl)-piperidin-4-yl]-acetic acid ethyl ester in acetonitrile (25 mL) is added 0.37 mL (2.9 mmol) of 3-chlorobenzoyl chloride. The mixture is stirred at room temperature for 2 hours then concentrated under reduced pressure. The residue is treated with a saturated aqueous solution of ammonium chloride and extracted with ethyl acetate. The combined organic phase is dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue is purified by flash silica gel chromatography to provide 0.590 g (56.7%) of {1-[4-chloro-2-(3-chloro-benzoylamino)-phenyl]-piperidin-4-yl}-acetic acid ethyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952004B2
Source datasetuspto-grants-2015_02
ORD IDord-a5312fabbe474119be3d663738ff823c
Source noteuspto-grants-2015_02