HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 70621110, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 2-{2-[(Benzyloxycarbonyl)amino]ethyl}-5-chloro-3-phenylisoindole-1-carboxylic acid ethyl ester | HCID 53708349 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 70621110 | HCID 70621110 | — |
Reaction Steps
4.8 G. of 2-{2-[(benzyloxycarbonyl)amino]-ethyl}-5-chloro-3-phenylisoindole-1-carboxylic acid ethyl ester are dissolved in 10 ml. of glacial acetic acid; 15 ml. of a solution of 33% hydrobromic acid in glacial acetic acid are added. The mixture is left to stand for 2 hours at room temperature with occasional shaking and then poured into 150 ml. of ether. The precipitated crystals are removed by filtration under suction and washed with ether. Recrystallization from ethanol yields 2-(2-aminoethyl)-5-chloro-3-phenylisoindole-1-carboxylic acid ethyl ester hydrobromide; melting point 230°-234° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03996374 |
| Source dataset | uspto-grants-1976_12 |
| ORD ID | ord-88eff4af46d34ec0a743bf1a7157bee2 |
| Source note | uspto-grants-1976_12 |