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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904281Generated: October 31, 2026

Acetic Acid → HCID 14553815, compound

https://huagongshe.com/reaction/1904281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 14553814HCID 14553814—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 14553815HCID 1455381594.5%

Reaction Steps

N-[3-(m-Phenoxyphenyl)-2-methylpropyl]-3-methoxymethyl-1,2,5,6-tetrahydropyridine (0.2 g) was dissolved in ethanol (20 ml), followed by addition of acetic acid (1 ml) thereto. To the resultant mixture, 5% palladium-carbon (0.2 g) was added at room temperature under nitrogen stream, and then hydrogenation was carried out under nitrogen stream. After absorption of hydrogen was completed, the catalyst was removed by filtration, and the filtrate was combined with 15% aqueous sodium hydroxide solution (20 ml) and extracted with diethyl ether. The ether extract was washed with saturated aqueous sodium chloride solution, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography to give N-[3-(m-phenoxyphenyl)-2-methylpropyl]-3-methoxymethylpiperidine (0.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04837236
Source datasetuspto-grants-1989_06
ORD IDord-a5765714c61242b299f0124502441b64
Source noteuspto-grants-1989_06