HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(1,1-Dimethylethyl) hydrogen L-glutamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Z-Glu-OtBu | HCID 6994036 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(1,1-Dimethylethyl) hydrogen L-glutamate | HCID 117505 | — |
Reaction Steps
To a solution of 25.0 g (74.1 mmol) (S)-2-(benzyloxycarbonylamino)pentanedioic acid 1-tert.-butyl ester (prepared according to Liebigs Ann. Chem. 1961, 646, 127) in 500 ml dry methanol were added 2.5 g 10% Pd/C, and the mixture was stirred over night at room temperature under an atmosphere of hydrogen. The catalyst was removed by filtration through celite and the filtrate was concentrated under reduced pressure. The remaining solid title compound was purified by stirring with a small amount of ethanol, filtered with suction, and dried in vacuo. Another crop (1.7 g) was obtained after concentration of the mother liquid and stirring of the residue with ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06528534B2 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-71008cb35c0747dc90dab36f4ad8ab56 |
| Source note | uspto-grants-2003_03 |