HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850708Generated: October 29, 2026
tert-Butyl 4-formylpiperidine-1-carboxylate → HCID 66934908, compound
https://huagongshe.com/reaction/1850708
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-formylpiperidine-1-carboxylate | HCID 1514430 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | (3-Benzyloxypropyl)triphenylphosphonium bromide | HCID 10929077 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66934908 | HCID 66934908 | — |
Reaction Steps
(3-Benzyloxypropyl)triphenylphosphonium bromide (2.88 g, 5.86 mmol) was suspended in 15 mL THF and cooled to 0° C. Sodium bis(trimethylsily)amide (1M in THF, 5.63 mL, 5.63 mmol) was added dropwise. The mixture turned deep orange. tert-Butyl 4-formylpiperidine-1-carboxylate (1 g, 4.69 mmol) in 3 mL THF was added after 5 minutes. Color faded to slight yellow. The reaction was stirred at RT for 1.5 hours, before quenching with saturated aqueous ammonium chloride solution. The aqueous layer was extracted twice with ethyl acetate. The organic layers were combined, washed with water and brine, dried over sodium sulfate, filtered, concentrated and purified by passing through a 40 gram Biotage silica gel cartridge using 20% EtOAc/hexanes to afford the product as colorless oil. NMR integration indicated >20:1 Z/E selectivity. LRMS calc: 345.2; obs: 346.5 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957062B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-b75d9182094d4cc09f788ac90b473939 |
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| Source note | uspto-grants-2015_02 |
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