HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13455633, compound → HCID 23700899, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13455633 | HCID 13455633 | — |
| Reactant | Sodium hydroxide ethanol | HCID 23692425 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23700899 | HCID 23700899 | 95% |
Reaction Steps
Under cooling with ice, a 0.48N sodium hydroxide-ethanol solution (54.2 ml) was added dropwise to an ethanol solution (70 ml) of ethyl trans-3-[(s)-1-(4-diphenylmethylpiperazine-1-yl carbonyl)-3-methylbutyl carbamoyl]oxirane-2-carboxylate (13.2 g) obtained above. After stirring at room temperature for 3 hours, the solvent was removed by distillation under reduced pressure, and the reaction mixture was further dried under reduced pressure to yield 12.4 g of sodium trans-3-[(s)-1-(4-diphenylmethylpiperazine-1-yl carbonyl)-3-methylbutylcarbamoyl]oxirane-2-carboxylate as a light yellow powder (yield: 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04507297 |
| Source dataset | uspto-grants-1985_03 |
| ORD ID | ord-c610a5579ad34d63bd07397037aba132 |
| Source note | uspto-grants-1985_03 |