HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dinitrophenol → HCID 178512180, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dinitrophenol | HCID 1493 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 131710601 | HCID 131710601 | — |
| Reactant | HCID 178512185 | HCID 178512185 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178512180 | HCID 178512180 | — |
Reaction Steps
In 30 ml. of DMF was dissolved in 1.0 g. of Z-β-Ala-Phe-Phe-Tyr-NH2, and using Pd-black as a catalyst, catalytic reduction was carried out for 6 hours. The catalyst was filtered off. To the filtrate was added a solution of Z-Arg(NO2)-ODNP in tetrahydrofuran (the dinitrophenyl ester prepared from 0.52 g. of Z-Arg(NO2)-OH and 0.30 g. of 2,4-dinitrophenol in 10 ml. of tetrahydrofuran by the DCC process). The mixture was stirred for 13 hours and the solvent was distilled off. To the residue was added 50 ml. of water and the resulting powder was collected by filtration and dried. Yield 1.01 g.(74.9 %); melting point: 192°-194°; α!D22 -11.1° (c=1.02 %, DMF)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04073890 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-83986e2ecd8041f884d669e9f56336fc |
| Source note | uspto-grants-1978_02 |