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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969547Generated: November 4, 2026

Ethyl 4-oxocyclohexanecarboxylate → HCID 17963321, compound

https://huagongshe.com/reaction/969547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-oxocyclohexanecarboxylateHCID 317638—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(3,4-Dichlorophenoxy)piperidineHCID 3732042—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 17963321HCID 1796332167.9%

Reaction Steps

4-(3,4-Dichlorophenoxy)piperidine (Method B, 1.44 g), ethyl 4-oxocyclohexanecarboxylate (1.0 g) and acetic acid (0.34 ml) were combined in THF 10 ml and the solution was cooled in ice. Sodium triacetoxy borohydride (1.45 g) was added and the mixture was stirred overnight and allowed to come to ambient temperature. The reaction mixture was poured onto a stirred saturated aq solution of sodium bicarbonate. The mixture was extracted with ethyl acetate thrice, the organic phases were washed with brine, dried, filtered and evaporated. The residue was purified on an SCX cartridge (International Sorbent Technology Isolute® Flash SCX-2), washed with methanol and then product eluted with 0.7M ammonia in methanol. Further purification by chromatography (silica, 90:9:1 DCM:methanol:triethylamine) gave the subtitle compound (1.59 g; MS [M+H]+ (APCI+) 400/402) as a mixture of cis/trans isomers.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307090B2
Source datasetuspto-grants-2007_12
ORD IDord-9df3cfb2dfec4536b00ed73d377aa138
Source noteuspto-grants-2007_12