HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458757Generated: October 29, 2026
Tetrahydrofuran → 1-Boc-4-Methylenepiperidine
https://huagongshe.com/reaction/458757
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl 4-oxopiperidine-1-carboxylate | HCID 735900 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | HCID 178418244 | HCID 178418244 | — |
| Product | 1-Boc-4-Methylenepiperidine | HCID 2756808 | — |
Reaction Steps
To a solution of 986 mg of methyltriphenylphosphonium bromide in 20 ml of tetrahydrofuran, 1.87 ml of 1.63 M n-butyl lithium/hexane solution was added dropwise at 0° C., under cooling with ice. The temperature then was immediately raised to room temperature, and the system was stirred for 50 minutes. The reaction liquid was again cooled to 0° C., to which a solution of 500 mg of t-butyl 4-oxotetrahydropyridine-1(2H)-carboxylate in 5 ml of tetrahydrofuran was added dropwise, followed by an hour's stirring at the same temperature. The reaction liquid was diluted with ethyl acetate, washed successively with saturated aqueous ammonium chloride solution and saturated brine, and dried over anhydrous sodium sulfate. Distilling the solvent off under reduced pressure, the resulting residue was purified on silica gel column chromatography (eluent: hexane/ethyl acetate=5/1) to provide 192 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192969B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-a70eb147709e4184a9e681b26e15ce89 |
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| Source note | uspto-grants-2007_03 |
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