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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044570Generated: October 30, 2026

Triethylamine → Ammonium hydroxide methanol

https://huagongshe.com/reaction/1044570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methoxyoxan-4-oneHCID 23533610—
ReactantHCID 68599587HCID 68599587—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 14923—
ProductHCID 11567437HCID 11567437—
ProductAmmonium hydroxide methanolHCID 218945081%

Reaction Steps

To a solution of (1R,3S)-3-isopropyl-3-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)carbonyl]cyclopentanamine hydrochloride (50 mg, 0.1 mmol), 3-methoxytetrahydro-4H-pyran-4-one (56 mg, 0.43 mmol), and triethylamine (0.07 mL, 0.5 mmol) in methylene chloride (2 mL) was added sodium triacetoxyborohydride (91 mg, 0.43 mmol). After being stirred at room temperature overnight, saturated NaHCO3 was added. The solution was extracted with methylene chloride three times. The combined extracts were dried (MgSO4), filtered, and concentrated. Purification by flash chromatography on silica gel (gradient 0-15% B over 15 min. Bottle A=1% NH4OH/3% MeOH/EtOAc, Bottle B=1% NH4OH/MeOH) afforded the desired compound. MS calculated for C26H35N2O3: (M+H) 427; found 427.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563582B2
Source datasetuspto-grants-2013_10
ORD IDord-ff5352a042c04a9b9c59c32de947f5a6
Source noteuspto-grants-2013_10