HuagongsheHuagongshe Chemistry Print Report · For research reference only
Binap, (A+-)- → (2R)-2-(4-methoxyphenyl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 2-(4-Methoxyphenyl)prop-2-enoic acid | HCID 14573787 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (2R)-2-(4-methoxyphenyl)propanoic acid | HCID 12398858 | 89% |
Reaction Steps
In a 100 ml autoclave, the inside atmosphere of which had previously been replaced with argon, were placed 0.36 g (2 mmoles) of p-methoxyatropic acid and 20 ml of methanol. Then, 7.5 mg (0.009 mmole) of Ru((+)-BINAP)-(O2CCH3)2 prepared according to the same manner as in Referential Example 3 except using (+)-BINAP in place of (-)-BINAP was added to the mixture to perform hydrogenation for 12 hours at a hydrogen pressure of 100 kg/cm2 and at a reaction temperature of 19° C. Thereafter, the solvent was distilled off to provide 0.32 g of (2R)-(-)-2-(p-methoxyphenyl)propionic acid. The yield was 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04962230 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-e6078a986a80410fbca8c058ab4aca0c |
| Source note | uspto-grants-1990_10 |