HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 2-Benzamido-4-chloro-5-[2-(p-aminophenoxy]-myristamido]-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-Benzamido-4-chloro-5-[2-(p-nitrophenoxy]-myristamido]-phenol | HCID 14122421 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Benzamido-4-chloro-5-[2-(p-aminophenoxy]-myristamido]-phenol | HCID 14122422 | — |
Reaction Steps
An amount of 670 g (1.10 mol) of 2-benzamido-4-chloro-5-[2-(p-nitrophenoxy]-myristamido]-phenol in the presence of 2370 ml of tetrahydrofuran, 47.8 g of morpholine, and 22 ml of Raney nickel is reduced in an autoclave at an initial hydrogen pressure of 10 MPa and a temperature of 40° C. After 90 min the theoretical amount of hydrogen is found to be taken up. The catalyst is filtered off. The filtrate is concentrated by evaporation to a volume of 1 l and then poured out in 4 l of ethanol. The precipitate is filtered off and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04822729 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-0206dc79aeec4df7b81c62b21cea761d |
| Source note | uspto-grants-1989_04 |