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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414889Generated: November 1, 2026

Acetic Acid → 359878-17-4

https://huagongshe.com/reaction/2414889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantN-MethylbenzylamineHCID 7669—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic acid methanolHCID 10129899—
Product359878-17-4HCID 9799308—

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 (M30 353), tr (A, MS) 3.982.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06815458B2
Source datasetuspto-grants-2004_11
ORD IDord-a457bd4c81c04c5d93c97c63ca6cbe56
Source noteuspto-grants-2004_11