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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-Methylcyclohexane-1-carboxaldehyde | HCID 11137168 | — |
| Reactant | (R)-Methyl 4-(1-aminoethyl)benzoate | HCID 17751897 | — |
| Product | (R)-methyl 4-(1-((1-methylcyclohexyl)methylamino)ethyl)benzoate | HCID 67395199 | 63.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382197B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-ef45cbb639e541f79c24a6a042314063 |
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| Source note | uspto-grants-2016_07 |
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