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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475700Generated: October 30, 2026

Acetic Acid → HCID 178420786, compound

https://huagongshe.com/reaction/475700

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopropylamineHCID 69828—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(Pyridin-3-yl)cyclohexan-1-oneHCID 20034907—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178420786HCID 178420786—

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyclopropyl amine (11.4 mL, 165 mmol) was added to a solution of 4-(3-pyridyl)cyclohexanone (19.2 g, 110 mmol) in DCE (360 mL) and acetic acid (12.6 mL, 220 mmol). The reaction mixture was cooled to 0° C. and NaBH(OAc)3 (46 g, 220 mmol) was added protionwise. After being stirred for 21 h at 23° C., the reaction was re-cooled to 0° C. and quenched with 1 M NaOH (200 mL). The aqueous layer was extracted with CH2Cl2 (2×200 mL) and the combined organic layers were washed with brine (300 mL), dried with MgSO4, filtered, and concentrated in vacuo. The crude mixture of cis and trans amines was purified by flash column chromatography (gradient elution, 40% EtOAc/hexanes (2.5% TEA)→70% EtOAc/hexanes (2.5% TEA)) to provide trans-N-cyclopropyl-4-(pyridine-3-yl)cyclohexylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637576B2
Source datasetuspto-grants-2014_01
ORD IDord-ab3a5afc98424cb69f7774bf64100ba4
Source noteuspto-grants-2014_01