HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696794Generated: November 1, 2026
4-Fluorobenzoyl chloride → HCID 11290310, compound
https://huagongshe.com/reaction/1696794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66618608 | HCID 66618608 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11290310 | HCID 11290310 | 45% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163775B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-b8ad61e895de4221a21e17cc19e75690 |
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| Source note | uspto-grants-2012_04 |
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