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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049100Generated: October 26, 2026

Acetic Acid → (R)-methyl 4-(1-((1-methylcyclohexyl)methylamino)ethyl)benzoate

https://huagongshe.com/reaction/1049100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethanolHCID 887—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-Methylcyclohexane-1-carboxaldehydeHCID 11137168—
Reactant(R)-Methyl 4-(1-aminoethyl)benzoateHCID 17751897—
Product(R)-methyl 4-(1-((1-methylcyclohexyl)methylamino)ethyl)benzoateHCID 6739519963.4%

Reaction Steps

To a solution of (R)-methyl 4-(1-aminoethyl)benzoate (0.12 g, 0.67 mmol) in methanol (2.97 mL, 73.33 mmol) was added 1-methylcyclohexane-1-carboxaldehyde (0.093 g, 0.74 mmol) and acetic acid (0.152 mL, 2.67 mmol). The reaction was stirred for 1 hour at room temperature whereupon sodium cyanoborohydride (63.1 mg, 1.00 mmol) was added and the mixture further stirred at room temperature overnight. The solvent was evaporated and the residual sodium cyanoborohydride quenched with saturated aqueous NaHCO3. The mixture was extracted into ethyl acetate, the organic layer washed with brine and the solvent evaporated to dryness. The residue obtained was purified via silica chromatography (0-5% MeOH/DCM) to afford the title compound as a colorless oil (123.0 mg, 63%). LC-MS: (FA) ES+ 290.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382197B2
Source datasetuspto-grants-2016_07
ORD IDord-ef45cbb639e541f79c24a6a042314063
Source noteuspto-grants-2016_07