HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Boc-ala-pro-OH
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[(1,1-Dimethylethoxy)carbonyl]-L-alanyl-L-proline phenylmethyl ester | HCID 13068139 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Boc-ala-pro-OH | HCID 11902919 | 83.8% |
Reaction Steps
The substance [24] was dissolved in ethanol (200 ml). 1 N NaOH (240 ml, 1.2 molar excess) was added dropwise at 0° C. and the mixture was stirred at room temperature. After two hours, 1 N NaOH (20 ml) was added and the mixture was further stirred for 30 minutes. The reaction mixture was neutralized with 1 N HCl (60 ml) at 0° C., and the ethanol was distilled off in vacuo. After twice washing the aqueous layer with ether (100 ml), 1 N HCl (200 ml) was added thereto at 0° C. The precipitate thus formed was filtered, washed completely and dried in vacuo. Recrystallization was effected from ethyl acetate (450 ml)-hexane to crystallize the substance [25] (47.92 g, yield: 83.8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04400316 |
| Source dataset | uspto-grants-1983_08 |
| ORD ID | ord-6ecc681bcbc94645b61bf154cafc569f |
| Source note | uspto-grants-1983_08 |