Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 15806771 | HCID 15806771 | — |
| Reactant | HCID 77833151 | HCID 77833151 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Rhodium | HCID 23948 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70562755 | HCID 70562755 | — |
Reaction Steps
A one liter autoclave was charged with 100 grams (0.341 mole) of α-acetamido-4-hydroxy-3-methoxy-cinnamic acid acetate, 254 milliliters of methanol, 170 milliliters of water and 13.7 (0.341 mole) sodium hydroxide. The slurry obtained was brought to about 25° C. and 40 psig. hydrogen pressure and a catalyst solution in 6 milliliters of benzene that was made from 0.025 gram (0.115 milli-equivalents) of rhodium 1,5-hexadiene chloride [Rh-(1,5-hexadiene)Cl]2 (J. Am. Chem. Soc. 86, 217 (1964)), and 0.058 gram (0.250 milli-equivalents) (+) methylphenyl-o-anisylphosphine (while preventing intrusion of air) is added. (The catalyst charge is equivalent to 0.0118 gram rhodium metal.) Hydrogen is absorbed immediately and is complete in 8 hours, giving the compound, N-acetyl-3-(4-hydroxy-3-methoxyphenyl)-alanine acetate, with 80 percent of such compound being present as the L enantiomorph and 20 percent being present as a D enantiomorph.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04005127 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-520ca381b57144c588e129e5730f644c |
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| Source note | uspto-grants-1977_01 |
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