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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2358902Generated: October 31, 2026

Acetic Acid → 1-(Cyclohexyl(methyl)amino)propan-2-ol

https://huagongshe.com/reaction/2358902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantFormaldehydeHCID 712—
Reactant2-Propanol, 1-(cyclohexylamino)-HCID 7630—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventEthyl AcetateHCID 8857—
SolventSodium HydroxideHCID 14798—
Product1-(Cyclohexyl(methyl)amino)propan-2-olHCID 277601—

Reaction Steps

To a stirred solution of 1-(cyclohexylamino)-propan-2-ol (crude 2.6 g) in DCE (30 mL) were added successively HCHO (35% in water, 2.1 mL, 24.8 mmol), Na(OAc)3BH (10.5 g, 49.6 mmol) and acetic acid (1 mL) at ice-cold conditions. The resulting mixture was allowed to stir at rt for 16 hours. The reaction was diluted with ethyl acetate and basified with 1N NaOH. The organic layer was separated, washed with water and brine, dried over Na2SO4, filtered and concentrated. The crude material was purified by chromatography on silica-gel (230-400 mesh) eluting with 5% MeOH/DCM to provide 1-(cyclohexyl(methyl)amino)propan-2-ol. Yield: 1.0 g 1H NMR (DMSO-d6) δ 4.11 (brs, 1 H), 3.65-3.57 (m, 1 H), 2.35-2.20 (m, 3 H), 2.19 (s, 3 H), 1.72-1.68 (m, 4 H), 1.57-1.54 (m, 1 H), 1.24-1.05 (m, 5 H), 1.01 (d, J=6 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685418B2
Source datasetuspto-grants-2014_04
ORD IDord-33bf0ff1cb054590bd6e40976ffcb724
Source noteuspto-grants-2014_04