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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415451Generated: October 31, 2026

Sodium Hydroxide → HCID 70562755, compound

https://huagongshe.com/reaction/1415451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 15806771HCID 15806771—
ReactantHCID 77833151HCID 77833151—
ReactantHCID 178418361HCID 178418361—
CatalystRhodiumHCID 23948—
SolventBenzeneHCID 241—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 70562755HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005127
Source datasetuspto-grants-1977_01
ORD IDord-520ca381b57144c588e129e5730f644c
Source noteuspto-grants-1977_01