HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587649Generated: October 29, 2026
1-Benzyl-4-piperidone → HCID 57459630, compound
https://huagongshe.com/reaction/587649
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 68108625 | HCID 68108625 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57459630 | HCID 57459630 | — |
Reaction Steps
To an anhydrous THF (50 mL) cooled at −70° C. stirred under nitrogen a 2.5 M solution of n-BuLi (4.22 mL, 10.54 mmol) was added. Then 2-bromo-5-fluoro-α,α-dimethyl-benzylalcohol (1.17 g, 5.02 mmol) [C.A.S.853271-16-6] was added dropwise. The resulting mixture was stirred at −70° C. for 2 h. Then a solution of 1-benzylpiperidin-4-one (1.33 g, 7.028 mmol) in anhydrous THF (10 ml) was added dropwise. Then, the resulting solution was stirred at r.t. overnight. The reaction mixture was poured into NH4Cl (aqueous sat. solution) at 5-10° C. The resulting aqueous solution was extracted with DCM. The organic layer was separated and concentrated in vacuo. The residue was purified by column chromatography (silica gel; heptane/EtOAc from 100/0 to 60/40 as eluent). The desired fractions were collected and concentrated in vacuo to yield intermediate D83 (0.4 g, 23%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09226930B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b2c37090df0a431fb792efc66cdd952c |
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| Source note | uspto-grants-2016_01 |
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