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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573480Generated: October 30, 2026

Acetic Acid → HCID 59264610, compound

https://huagongshe.com/reaction/573480

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
Reactant4-(4-TRIFLUOROMETHYLPHENYL)BENZYLAMINEHCID 3729155—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantEthyl 2-methyl-2-(4-oxo-1-piperidinyl)propanoateHCID 59264612—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59264610HCID 59264610—

Reaction Steps

A mixture of ethyl 2-methyl-2-(4-oxo-1-piperidinyl)propanoate (Int. A4) (25.6 g, 1.2 equiv), {[4′-(trifluoromethyl)-4-biphenylyl]methyl}amine (Int. A1) (31.1 g, 1.0 equiv), DCE (400 ml) and acetic acid (6.3 ml, 1.1 equiv) was stirred at room temperature under nitrogen. Sodium triacetoxyborohydride (33.5 g, 1.5 equiv) was added and stirring continued for 19 hours. Aqueous sodium carbonate (2M solution, excess) was added and stirred for 1.5 h, then the mixture was extracted with a mixture of diethyl ether and THF. The organic extracts were backwashed with water and brine, filterered through a pad of silica gel, dried over sodium sulfate and evaporated in vacuo. The desired product was obtained as a white solid (44.2 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029383B2
Source datasetuspto-grants-2015_05
ORD IDord-6bcdae324edc44bfb294c7b50b006e06
Source noteuspto-grants-2015_05