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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2122040Generated: November 1, 2026

Hydrochloric Acid → 1-Benzyl-4-methylpiperidin-3-ol

https://huagongshe.com/reaction/2122040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHydrogen PeroxideHCID 784—
ReactantBoron trifluoride etherateHCID 8000—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
Reactant1-Benzyl-4-methyl-1,2,3,6-tetrahydropyridineHCID 6421572—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Benzyl-4-methylpiperidin-3-olHCID 2195538479%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the product from Method B (72.45 grams/0.387 mol) dissolved in 240 mL of THF was added 21.4 grams of NaBH4 and the mixture cooled to 0° C. A solution of borontrifluoride etherate (109.4 mL dissolved in 200 mL of THF) was then added dropwise over 1.5 hours. Once added, the reaction mixture was brought to room temperature and stirred for 2 hours. The reaction was again cooled to 0° C. and 29.3 mL of water were added dropwise over 15 minutes followed by dropwise addition of 2N sodium hydroxide (97.5 mL) over 20 minutes. The resulting mixture stirred at 0° C. for 40 minutes and was then brought to room temperature. Hydrogen peroxide (30%) (97.5 mL) was added dropwise at a rate so as not to exceed 50° C. in the reaction mixture (approximately 30 minutes). When the addition was complete, the reaction mixture stirred for 10 minutes, then was cooled to 0° C. Concentrated hydrochloric acid (97.5 mL) was added over 5 minutes, the reaction mixture was reduced to one third its volume in vacuo, and the pH adjusted to 9-10 with 6N sodium hydroxide (aq). The resulting mixture was extracted three times with ether, the combined ether layers dried over MgSO4 and evaporated to dryness in vacuo affording 65.32 grams (79%) of the title compound as yellow oil. LRMS: 206.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696567B2
Source datasetuspto-grants-2004_02
ORD IDord-964ac29ae1cf47fba8c33cca2a0d76d5
Source noteuspto-grants-2004_02