HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387749Generated: October 30, 2026
1-Bromo-4-phenylmethoxybenzene → (R)-4-(4-benzyloxy-phenyl)-1-(1-phenyl-ethyl)-piperidin-4-ol
https://huagongshe.com/reaction/1387749
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Bromo-4-phenylmethoxybenzene | HCID 138835 | — |
| Reactant | (R)-1-(1-phenylethyl)tetrahydro-4(1H)-pyridinone | HCID 13147386 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | (R)-4-(4-benzyloxy-phenyl)-1-(1-phenyl-ethyl)-piperidin-4-ol | HCID 9886545 | 121.8% |
Reaction Steps
175.2 g (666 mmol) 4-benzyloxybromobenzene was dissolved in 1.4 L dry THF (MS 4 A) under argon. The solution was cooled to −75° C. and a solution of 416 mL 1.6 M butyllithium (666 mmol) in hexane was added during 40 minutes. After stirring for 1 hour a solution of 113 g (555 mmol) (R)-1-(1-phenyl-ethyl)-piperidin-4-one in 400 mL THF was added during 1hour at −75° C. The mixture was stirred for another 1 hour and, after heating to room temperature, poured into 1.5 L of ice-water. The mixture was extracted with 1 L ethyl acetate. The organic phase was washed with 1 L of a half-saturated NaCl solution, dried over Na2SO4 and concentrated to yield 262 g of (R)-4-(4-benzyloxy-phenyl)-1-(1-phenyl-ethyl)-piperidin-4-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06268499B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-c1278418fb3842db8d38a45515576b49 |
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| Source note | uspto-grants-2001_07 |
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