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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866866Generated: October 27, 2026

Ethanol → HCID 20318877, compound

https://huagongshe.com/reaction/866866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMagnesium orthosilicateHCID 66225—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 20318874HCID 20318874—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventBenzene methyl ketoneHCID 22015841—
ProductHCID 20318877HCID 20318877—

Reaction Steps

A mixture of 3.78 g. (0.1 mole) of sodium borohydride in 25 ml. of anhydrous ethanol was stirred at room temperature. A solution of 8.16 g. (0.02 mole) of 2-(p-fluorophenyl)-2-{3-[4-(p-fluorobenzoyl)piperidino]propyl}-1,3-dioxolane in 10 ml. of anhydrous ethanol was slowly added dropwise so as to maintain a controlled evolution of gas. After the addition was complete the mixture was allowed to stir at room temperature for 16 hr. A large excess of water was added and the mixture was extracted several times with benzene. The benzene extracts were dried with anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and a glass-like residue was obtained. The residue was dissolved in benzene and placed on a magnesium silicate column. Using a benzene-acetone gradient solution, the product was obtained. Recrystallization of the solid product from methanol-isooctane gave 6.5 g. (78%) of white solid melting at 114°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101662
Source datasetuspto-grants-1978_07
ORD IDord-f1abb041d5b74f3e9f0307837180aa03
Source noteuspto-grants-1978_07