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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872399Generated: November 1, 2026

Water → HCID 21182312, compound

https://huagongshe.com/reaction/1872399

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 4-(piperazin-1-yl)benzoateHCID 2761178—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 21182250HCID 21182250—
CatalystTitanium isopropoxideHCID 11026—
SolventEthanolHCID 702—
ProductHCID 21182312HCID 2118231222.4%

Reaction Steps

A mixture of 1-(4-n-Hexyloxyphenyl)-4-piperidone (0.823 g), 1-(4-Ethoxycarbonylphenyl)piperazine (0.7 g), and titanium(IV) isopropoxide (1.11 ml) was stirred at room temperature. After 1 hour, the IR spectrum of the mixture showed no ketone band, and the viscous solution was diluted with absolute ethanol (3 ml). Sodium cyanoborohydride (0.121 g) was added, and the solution was stirred for 3 hours. Water (3 ml) was added with stirring, and the resulting in organic precipitate was filtered and washed with ethanol. The filtrate was extracted with ethyl acetate. The organic layer was taken and dried over magnesium sulfate. The magnesium sulfate was filtered off, and filtrate was evaporated under reduced pressure to give Ethyl 4-[4-[1-(4-n-hexyloxyphenyl)piperidin-4-yl]piperazine-1-yl]benzoate (331 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107458
Source datasetuspto-grants-2000_08
ORD IDord-5eac68a404ee48ffb8a06698a62f7870
Source noteuspto-grants-2000_08