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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855626Generated: November 2, 2026

Acetic Acid → HCID 59264602, compound

https://huagongshe.com/reaction/1855626

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
Reactant4-(4-TRIFLUOROMETHYLPHENYL)BENZYLAMINEHCID 3729155—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 59264606HCID 59264606—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59264602HCID 5926460267.1%

Reaction Steps

A mixture of methyl 2-methyl-2-(4-oxo-1-piperidinyl)propanoate (Int. A3) (14.28 g, 1 equiv), {[4′-(trifluoromethyl)-4-biphenylyl]methyl}amine (Int. A1) (19.6 g, 0.85 equiv), DCE (300 ml), acetic acid (3.8 ml, 0.90 equiv) and sodium triacetoxyborohydride (20.7 g, 1.25 equiv) was stirred at room temperature under nitrogen for 17.5 h. Aqueous sodium carbonate (2M solution, excess) was added and stirred for 4 h, then the mixture was extracted with a mixture of diethyl ether and THF. The organic extracts were backwashed with water and brine, dried over sodium sulfate and filterered through a pad of silica gel which was rinsed with 2.5% methanol in DCM. After evaporation in vacuo, the crude product was crystallised from ether/hexane, finally at ice bath temperature, which after drying yielded a white solid (20.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962633B2
Source datasetuspto-grants-2015_02
ORD IDord-c7f0c6194da7438b92d91a55ba934228
Source noteuspto-grants-2015_02