HuagongsheHuagongshe Chemistry Print Report · For research reference only
Binap, (A+-)- → 3-Phenylbutyric acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | (2Z)-3-(3-Methylphenyl)-2-propenoic acid | HCID 2529400 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Phenylbutyric acid | HCID 20724 | 100% |
Reaction Steps
In a 100 ml autoclave, the inside atmosphere of which had previously been replaced with argon, were placed 0.32 g (2 mmoles) of (Z)-3-methylcinnamic acid and 20 ml of methanol. Then, 2.9 mg (0.0034 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 70 hours at a hydrogen pressure of 104 kg/cm2 and at a reaction temperature of 25° C. Thereafter, the solvent was distilled off to provide 0.32 g of 3-phenylbutyric acid. The yield was 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04962230 |
| Source dataset | uspto-grants-1990_10 |
| ORD ID | ord-1f6d0cd8c9c146658d7e487e6671b2e3 |
| Source note | uspto-grants-1990_10 |