HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 70567512, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 70566818 | HCID 70566818 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 70567512 | HCID 70567512 | — |
Reaction Steps
To 3.58 grams of methyl carbobenzoxy-L-phenylalanyl-3-amino-1-adamantanecarboxylate dissolved in 10 ml of acetic acid is added 15 ml of a 5 M solution of hydrogen bromide in acetic acid, and the reaction mixture is allowed to stand for one hour at room temperature. The solvent is removed by distillation under vacuum and the residue is shaken with two 100 ml portions of hexane, then 100 ml of ether, to give methyl L-phenylalanyl-3-amino-1-adamantanecarboxylate hydrobromide which has the following structural formula ##STR14##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04273704 |
| Source dataset | uspto-grants-1981_06 |
| ORD ID | ord-007d72f0184344c3838657551f8a6635 |
| Source note | uspto-grants-1981_06 |