Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | L-Phenylalanine, hydrochloride (1:1) | HCID 12000150 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | L-Phenylalanine | HCID 6140 | 61% |
Reaction Steps
To a still there were charged the mother liquor and acetic acid wash of Example I and the mixture was concentrated to 45% solids at 55° C. The contents of the still were then transferred to a hydrolyzer and combined with the mother liquor of Example II and there were added 0.50 mole HCl and 1.60 moles water. The mixture was then heated to 105° C. with stirring while low boilers were removed. The solution was held at 105° C. for 13 hours to effect hydrolysis. The mixture was transferred to a crystallizer where the temperature was adjusted to 80° C. and 3.27 moles of HCl were added. The mixture was then cooled to 50° C. over 3 hours and then adjusted to 5° C. L-phenylalanine hydrochloride was then centrifuged from the mixture. To the L-phenylalanine hydrochloride dissolved in 157.6 g. of deionized water was added 0.66 mole sodium hydroxide in order to adjust the pH of the solution to the isoelectric point (pH 5.0). At the isoelectric point there was afforded a 61% yield of available L-phenylalanine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04348317 |
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| Source dataset | uspto-grants-1982_09 |
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| ORD ID | ord-699c593adabf47beb537d22a77354c88 |
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| Source note | uspto-grants-1982_09 |
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