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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1661192Generated: November 2, 2026

Triethylamine → HCID 11739424, compound

https://huagongshe.com/reaction/1661192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantHCID 66618519HCID 66618519—
SolventDichloromethaneHCID 6344—
ProductHCID 11739424HCID 1173942482%

Reaction Steps

4-Fluorobenzoyl chloride (53 mL, 0.45 mmol) was added at 0° C. to a solution of (S)-piperidine-3-carboxylic acid (4-fluoro-phenyl)-amide hydrochloride (0.116 g, 0.45 mmol) and triethylamine (131 mL, 0.94 mmol) in dichloromethane (3 mL), under nitrogen atmosphere. The reaction mixture was kept under stiffing at R.T. for 2.5 h, the solvent was evaporated and the residue was diluted with water and ethyl acetate. The phases were separated and the organic layer was washed with HCl 1N (10 mL), with Na2CO3 2M (aq.) (10 mL) and with brine (10 mL). The organic layer was dried over sodium sulphate and concentrated under reduced pressure to give 0.127 g of (S)-1-(4-fluoro-benzoyl)-piperidine-3-carboxylic acid (4-fluoro-phenyl)-amide as a white solid. Yield: 82%; mp=163-164° C.; [α]D20=+54.7° (c=0.995, CHCl3); LCMS (Tr): 6.68 min (Method A); MS (ES+) gave m/z: 345.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030331B2
Source datasetuspto-grants-2011_10
ORD IDord-1b1a77431bf343439abe55b3f254a67d
Source noteuspto-grants-2011_10