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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172733Generated: November 1, 2026

4-Fluorobenzoyl chloride → HCID 11290310, compound

https://huagongshe.com/reaction/1172733

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 66618608HCID 66618608—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11290310HCID 1129031045%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 3-(4-Fluoro-phenylethynyl)-piperidine hydrochloride (0.14 g, 0.58 mmol) in THF (2.3 ml, 0.5M) was added DIEA (0.5 ml, 2.92 mmol). The reaction mixture was cooled to 0° C. and 4-Fluoro-benzoyl chloride (0.139 g-0.87 mmol) was slowly added. The reaction was to go up to R.T and stirred for 24 h. The solution was concentrated and DCM was added following by HCl 1N. The aqueous phase was separated and organic phase was extracted twice with HCl 1N and twice with water, dried over Na2SO4, filtered and concentrated. The crude product was purified by flash chromatography (DCM/MeOH: 98/2) to afford 0.86 mg (45%) of (4-Fluoro-phenyl)-[3-(4-fluoro-phenylethynyl)-piperidin-1-yl]-methanone as a brown oil. Rf=0.39 (DCM/MeOH: 98/2); LCMS (Tr): 4.14 min (Method C); MS (ES+) gave m/z: 326.2;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834035B2
Source datasetuspto-grants-2010_11
ORD IDord-c6eab26ad3c648dd98050d04759c778d
Source noteuspto-grants-2010_11