HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 85810079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | HCID 14329130 | HCID 14329130 | — |
| Reactant | Acetic Acid Mixture with Hydrobromic Acid | HCID 21893785 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 85810079 | HCID 85810079 | — |
Reaction Steps
A well stirred solution of 45.0 g. (0.13 mole) of carbobenzyloxyglycine 2,2,2-trichloroethyl ester in 100 ml. of glacial acetic acid is cooled to 20° and 100 ml. of 5N HBr-CH3CO2H is added. After 10 minutes, a vigorous evolution of gas occurs. The reaction mixture is stirred at room temperature for two hours. The mixture is then diluted with dry ethyl ether and the precipitate is filtered. The product is crystallized from acetonitrile to give aminoacetic acid 2,2,2-trichloroethyl ester, hydrobromide as white crystals; m.p. 238°-240° (d); 29.5 g. (78.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04172148 |
| Source dataset | uspto-grants-1979_10 |
| ORD ID | ord-02c4edb3844f40b6bbb0e754e277c99c |
| Source note | uspto-grants-1979_10 |