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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634322Generated: October 31, 2026

Sodium Bicarbonate → (2S,3S)-3-(2-methoxy-5-(trifluoromethyl)benzyl)amino-2-phenylpiperidine

https://huagongshe.com/reaction/1634322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-Methoxy-5-(trifluoromethyl)benzaldehydeHCID 2779272—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(2S,3S)-2-Phenylpiperidin-3-amine dihydrochlorideHCID 69654807—
SolventDichloromethaneHCID 6344—
Product(2S,3S)-3-(2-methoxy-5-(trifluoromethyl)benzyl)amino-2-phenylpiperidineHCID 9889280—

Reaction Steps

To a stirred suspension of Compound 1 (150 mg, 0.60 mmol) and Compound 4 (123 mg, 0.60 mmol) in dry CH2Cl2 (6 ml) was added NaBH(OAc)3 (179 mg, 0.84 mmol) portionwise under nitrogen at room temperature. The reaction mixture was stirred at room temperature for 3.5 hr. This was basified with sat. NaHCO3 aq., extracted with CH2Cl2, dried with MgSO4, and concentrated to give crude (2S,3S)-3-(2-methoxy-5-(trifluoromethyl)benzyl)amino-2-phenylpiperidine as a colorless oil. This was purified with chromatography to give pure (2S,3S)-3-(2-methoxy-5-(trifluoromethyl)benzyl)amino-2-phenylpiperidine as a colorless oil (95 mg). This was diluted with ethyl acetate, added HCl-MeOH, and concentrated. The white solid was recrystallized from MeOH-ether to give Compound 5 as a white crystalline (85 mg, 32.4%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506775B1
Source datasetuspto-grants-2003_01
ORD IDord-add1c2ce350849f787391b387b1b576f
Source noteuspto-grants-2003_01