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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270560Generated: October 27, 2026

Triethylamine → Ammonium hydroxide methanol

https://huagongshe.com/reaction/270560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-Methyloxan-4-oneHCID 14170926—
ReactantHCID 68930927HCID 68930927—
SolventDichloromethaneHCID 6344—
ProductAmmonium HydroxideHCID 14923—
ProductAmmonium hydroxide methanolHCID 218945081%
ProductHCID 68597077HCID 68597077—

Reaction Steps

To a solution of 1-{[(1S,3R)-3-amino-1-isopropylcyclopentyl]carbonyl}-4-[2-(trifluoromethyl)phenyl]piperidin-4-ol hydrochloride (50 mg, 0.1 mmol), 3-methyltetrahydro-4H-pyran-4-one (39 mg, 0.34 mmol), and triethylamine (0.048 mL, 0.34 mmol) in methylene chloride (5 mL) was added sodium triacetoxyborohydride (73 mg, 0.34 mmol). After being stirred overnight at room temperature, a saturated solution of 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 (0-20% B over 15 min. Bottle A=1% NH4OH/2% MeOH/EtOAc, Bottle B=1% NH4OH/MeOH) afforded the desired product as an oil. MS calculated for C27H39F3N2O3: (M+H) 497; found 497.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07449467B2
Source datasetuspto-grants-2008_11
ORD IDord-16e8affef9cc44f090a7f58699380b36
Source noteuspto-grants-2008_11