HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Hydroxide → Ethyl [4-(methoxymethyl)piperidin-4-yl]phenylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 53960004 | HCID 53960004 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Ethyl [4-(methoxymethyl)piperidin-4-yl]phenylcarbamate | HCID 54010374 | 81.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03998834 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-c1fe4ae7fd5a4906b81f60f1ab6eb24a |
| Source note | uspto-grants-1976_12 |