HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867396Generated: October 25, 2026
1-Benzyl-3-methyl-4-piperidone → 1-Benzyl-3-methylpiperidin-4-ol
https://huagongshe.com/reaction/1867396
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Benzyl-3-methyl-4-piperidone | HCID 560965 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Benzyl-3-methylpiperidin-4-ol | HCID 13611492 | 102.3% |
Reaction Steps
Benzyl-3- methyl-piperidin-4-one (2.0 g, 10 mmol) was dissolved in MeOH (10 ml), cooled to 0° C. and sodium borohydride (0.2 g, 5 mmol) was added portionwise. The reaction was allowed to reach room temperature and stirred overnight after which time the solvent was removed under vacuum, the residue redissolved in CH2Cl2, washed with water, dried (Na2SO4) and concentrated to afford the title compound (2.1 g, quant), a 3:1 mixture of diasteriomers (trans:cis) as gum. MS: 206.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07632829B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-11463f45e6604c3e94b264e4044cc1bd |
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| Source note | uspto-grants-2009_12 |
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