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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Methoxy-5-(trifluoromethyl)benzaldehyde | HCID 2779272 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | (2S,3S)-2-Phenylpiperidin-3-amine dihydrochloride | HCID 69654807 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2S,3S)-3-(2-methoxy-5-(trifluoromethyl)benzyl)amino-2-phenylpiperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06506775B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-add1c2ce350849f787391b387b1b576f |
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| Source note | uspto-grants-2003_01 |
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