Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Aspartic Acid | HCID 5960 | — |
| Reactant | L-Tyrosine | HCID 6057 | — |
| Reactant | L-Phenylalanine | HCID 6140 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | L-Glutamic Acid | HCID 33032 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 131719727 | HCID 131719727 | — |
Reaction Steps
750 ml of tetramethylene sulfone was heated to 190° C. in an inert nitrogen atmosphere in a 4 liter flask with stirring. 294 g of glutamic acid was added and the mixture was heated for one-half hour. 266 g of aspartic acid was added and the mixture heated as rapidly as possible to 190° C. and held there for 15 minutes. 362 g of tyrosine was added and the mixture heated at 190° C. for 3 hours. 330 g of phenylalanine was added and the mixture heated at 190° C. for 1.5 hours. The hot melt was then poured into 5 liters of water with vigorous stirring. After stirring for about 1 hour, the mixture was filtered and the filtrate discarded. The cake was reslurried in 5 liters of water, filtered and the cake was again reslurried in 5 liters of water. The pH of the slurry (at 25° C.) was adjusted to 8 using 40% sodium hydroxide solution. The mixture was filtered and the cake washed with a small amount of water. The washes and filtrate are combined and evaporated to dryness in vacuo to give Glu/Asp/Tyr/Phe proteinoid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05578323 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-bf6d88ef78834b8e9591108c5275fa46 |
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| Source note | uspto-grants-1996_11 |
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