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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634329Generated: October 27, 2026

Acetic Acid → (2S,3S)-1-tert-Butoxycarbonyl-3-(5-(1,1-difluoroethyl)-2-(trifluoromethoxy)benzyl)amino-2-phenylpiperidine

https://huagongshe.com/reaction/1634329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 3-amino-2-phenylpiperidine-1-carboxylateHCID 10214733—
Reactant5-(1,1-Difluoroethyl)-2-(trifluoromethoxy)benzaldehydeHCID 18677608—
SolventDichloromethaneHCID 6344—
Product(2S,3S)-1-tert-Butoxycarbonyl-3-(5-(1,1-difluoroethyl)-2-(trifluoromethoxy)benzyl)amino-2-phenylpiperidineHCID 70001814156.8%

Reaction Steps

To a stirred solution of Compound 12 (500 mg, 1.81 mmol) and Compound 25 (552 mg, 2.17 mmol) in dry CH2Cl2 (10 ml) was added sodium triacetoxyborohydride (1.15 g, 5.43 mmol) portionwise at room temperature. Then to this was added acetic acid (109 mg, 1.81 mmol) at same temperature. The reaction mixture was stirred at room temperature for 66 h. The reaction mixture was basified to pH10-11 with 10% NaOH aq. with ice-cooling. The organic layer was separated and the aqueous layer was extracted with CH2Cl2. The combined solution was washed with brine, dried (MgSO4), and concentrated in vacuo to give crude product (1.46g) as a pale yellow oil. This was employed for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506775B1
Source datasetuspto-grants-2003_01
ORD IDord-3b0cb54ca43b4f278cda313bc317fe38
Source noteuspto-grants-2003_01