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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606204Generated: October 30, 2026

Ethyl Acetate → HCID 22248099, compound

https://huagongshe.com/reaction/606204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium potassium tartrate tetrahydrateHCID 2724148—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 22248107HCID 22248107—
SolventDiethyl EtherHCID 3283—
ProductHCID 22248099HCID 2224809979%

Reaction Conditions

Temperature-20 °C

Reaction Steps

After dissolving 247 mg of ethyl 1-(2-methoxy-3-pyridinylmethyl)-4-(2-phenylethyl)piperidine-4-carboxylate in 10 ml of diethyl ether, the solution was cooled to −20° C. and 1 ml of diisobutylaluminium hydride (1.5 M, toluene solution) was added dropwise. The mixture was stirred for 4 hours while slowly raising the temperature to room temperature, and then approximately 10 ml of a saturated aqueous solution of potassium sodium (+)-tartrate tetrahydrate and approximately 10 ml of ethyl acetate were added and the mixture was stirred for 10 minutes at room temperature. The organic layer was separated off and the aqueous layer was extracted with ethyl acetate. The organic layers were combined and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by NH silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain the title compound (173 mg, 79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915274B2
Source datasetuspto-grants-2011_03
ORD IDord-ddfd939309374b058093a82b3162471d
Source noteuspto-grants-2011_03