HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380486Generated: October 30, 2026
(3-Bromopropyl)benzene → 1-Benzyl-4-(3-phenylpropyl)piperidin-4-ol
https://huagongshe.com/reaction/380486
Participants
| Role | Name | HCID | Charge |
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| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-Benzyl-4-(3-phenylpropyl)piperidin-4-ol | HCID 22624478 | 77.3% |
Reaction Steps
To a solution of 3.8 mL (25 mmol) of 1-bromo-3-phenyl propane in 200 mL of ether at −78° C. was slowly added 30 mL (50 mmol) of t-BuLi (1.7 M in pentane). The reaction mixture was warmed to −20° C. for 15 min, then it was recooled to −78° C. To this reaction mixture was slowly added a solution of 2.61 g (13.8 mmol) of 1-benzyl-4-piperidone in 20 mL of ether. After 15 min, the reaction mixture was poured into, 200 mL of sat'd NH4Cl solution. The reaction mixture was extracted with ethyl acetate and the combined organic fractions were washed with sat'd NaCl solution, dried over MgSO4 filtered and the filtrate was concentrated. The residue was purified by chromatography (silica, hexanes: ethyl acetate, 1:1) to give 3.3 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06303593B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-cf6892b86a5141ed959c210795866f75 |
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| Source note | uspto-grants-2001_10 |
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