HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19352281, compound → HCID 10868373, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19352281 | HCID 19352281 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 10868373 | HCID 10868373 | — |
Reaction Steps
The step consists in the catalytic hydrogenation of 3-benzyloxycarbonylamino-5-(2,3-dimethoxyphenyl)-2,5-dihydrofuran-2-one, for example with palladium on carbon as catalyst in alcoholic medium, thus obtaining directly in a single step the deprotected 2-amino-4-(2,3-dimethoxyphenyl)butyric acid. The reaction takes place in nearly quantitative yields. The reaction, as already discussed in the above process, can be carried out under enantioselectivity conditions, to obtain 2-amino-4-(2,3-dimethoxyphenyl)butyric acid in an optically active form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06034277 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-bf4172861429425fb8a870b76e2a7a43 |
| Source note | uspto-grants-2000_03 |