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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973848Generated: November 1, 2026

Ammonium Hydroxide → Ethyl [4-(methoxymethyl)piperidin-4-yl]phenylcarbamate

https://huagongshe.com/reaction/1973848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 53960004HCID 53960004—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductEthyl [4-(methoxymethyl)piperidin-4-yl]phenylcarbamateHCID 5401037481.4%

Reaction Steps

A solution of 14.2 parts of (phenylmethyl) 4-[(ethoxycarbonyl)phenylamino]-4-(methoxymethyl)-1-piperidinecarboxylate and 1.8 parts of ammonium hydroxide in 120 parts of methanol is hydrogenated at normal pressure and at room temperature with 4 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is dissolved in 75 parts of trichloromethane. The solution is washed twice with water, dried, filtered and evaporated, yielding 7.9 parts (81.4%) of ethyl [4-(methoxymethyl)-4-piperidinyl]phenylcarbamate as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998834
Source datasetuspto-grants-1976_12
ORD IDord-c1fe4ae7fd5a4906b81f60f1ab6eb24a
Source noteuspto-grants-1976_12