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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573481Generated: November 1, 2026

Acetic Acid → HCID 59264607, compound

https://huagongshe.com/reaction/573481

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(4-trifluoromethoxyphenyl)benzylamine HydrochlorideHCID 22928457—
ReactantEthyl 2-methyl-2-(4-oxo-1-piperidinyl)propanoateHCID 59264612—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 59264607HCID 59264607—

Reaction Steps

A mixture of ethyl 2-methyl-2-(4-oxo-1-piperidinyl)propanoate (Int. A4) (1.09 g, 1.2 equiv), ({4′-[(trifluoromethyl)oxy]-4-biphenylyl}methyl)amine hydrochloride (Int. A2) (1.28 g, 1.0 equiv), DCE (21 ml) and acetic acid (0.27 ml, 1.1 equiv) was stirred at room temperature under nitrogen. Sodium triacetoxyborohydride (1.42 g, 1.5 equiv) was added and stirring contined for 3 hours. Aqueous sodium carbonate (2M solution, excess) was added and stirred for 45 min, then the mixture was partitioned with a mixture of diethyl ether/THF and water. The organic extracts were backwashed with water and brine, and dried over sodium sulfate and evaporated in vacuo. The desired product was obtained as a light yellow solid (2.14 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029383B2
Source datasetuspto-grants-2015_05
ORD IDord-6a249da4753145f6ade8ada9c016e1d3
Source noteuspto-grants-2015_05