HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172727Generated: October 25, 2026
4-Fluorobenzoyl chloride → Ethyl 1-(4-fluorobenzoyl)piperidine-3-carboxylate
https://huagongshe.com/reaction/1172727
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl nipecotate | HCID 98969 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1-(4-fluorobenzoyl)piperidine-3-carboxylate | HCID 2905457 | 33% |
Reaction Steps
To a mixture of Ethyl nipecotate (2 g, 12.72 mmol) in THF (25 ml, 0.5M) was added DIEA (4.79 ml, 27.99 mmol). The reaction mixture was cooled to 0° C. and 4-Fluoro-benzoyl chloride (2.5 g-15.76 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 to afford 1.15 g (33%) of 1-(4-Fluoro-benzoyl)-piperidine-3-carboxylic acid ethyl ester as a colorless oil which can be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834035B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-361b4862e0384bc3911ea6998ea6d09e |
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| Source note | uspto-grants-2010_11 |
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