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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929723Generated: November 4, 2026

Methanol → 1-methyl-N-[(4-methylphenyl)methyl]piperidin-4-amine

https://huagongshe.com/reaction/929723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantN-MethylbenzylamineHCID 7669—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventAcetic acid methanolHCID 10129899—
Product1-methyl-N-[(4-methylphenyl)methyl]piperidin-4-amineHCID 11993862—

Reaction Steps

Methanol (50 ml) was added to an Erlenmeyer flask and acetic acid was added under stirring until pH 5. Methylbenzylamine (1.0 g, 8.8 mmol) and 1-Methyl-4-piperidone (1.1 g, 8.8 mmol) were added to a 100 ml round-bottomed flask and dissolved in the methanol/acetic acid (40 ml) solution previously made. The reaction mixture was stirred for 5 min and NaCNBH3 (0.83 g, 13.2 mmol) was added slowly under stirring. After 20 hours the reaction was concentrated and transferred to a separatory funnel containing dichloromethane and distilled water. The aqueous phase was made basic by addition of Na2CO3. The aqueous phase was extracted twice with dichloromethane. The combined organic layers were collected and dried with Na2SO4. Concentration afforded the title compound. Yield (crude): 98%. UV/MS 89/88 (M+ 353), tr (A, MS) 3.982.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296694B2
Source datasetuspto-grants-2016_03
ORD IDord-d370ae7c540d49f5b4f44f181940633a
Source noteuspto-grants-2016_03