HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403827Generated: November 1, 2026
1-((Phenylmethoxy)carbonyl)-3-piperidinebutanoic acid → Phenylmethyl 3-(4-hydroxybutyl)-1-piperidinecarboxylate
https://huagongshe.com/reaction/2403827
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-((Phenylmethoxy)carbonyl)-3-piperidinebutanoic acid | HCID 44890831 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Phenylmethyl 3-(4-hydroxybutyl)-1-piperidinecarboxylate | HCID 58306139 | — |
Reaction Steps
To a solution of 4-(1-{[(phenylmethyl)oxy]carbonyl}-3-piperidinyl)butanoic acid (5.01 g, 16.41 mmol) in dry THF (40 ml) at 0° C. under nitrogen was added a solution of Borane-THF complex, (1M soln. in THF) (49.2 ml, 49.2 mmol), dropwise over 1 hour. The mixture was allowed to stir at 0° C. and gradually allowed to warm to rt over 20 hours. The mixture was cooled in an ice bath and cautiously quenched with dropwise addition of MeOH (20 ml) stirred in the cold bath for 2 hours then quenched further with 10% 2N HCl/MeOH (20 ml), stirred for 1 hour at rt and evaporated under reduced pressure. The residue was co-evaporated with methanol several times.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802684B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-a5b01dad871642769e7300f04eefed21 |
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| Source note | uspto-grants-2014_08 |
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