Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Tyrosine | HCID 6057 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1-Octanol | HCID 957 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66739249 | HCID 66739249 | — |
Reaction Steps
9.06 g of tyrosine was dissolved in a solution of 10 g of concentrated sulfuric acid, 20 mL water, 10 mL of octanol, and 200 mL of toluene in a 500 mL round bottom flask equipped with a condenser and a Dean-Stark apparatus. The resulting solution was heated at reflux temperature until no more water could be distilled. The resulting solution was then cooled to room temperature and washed with saturated aqueous sodium bicarbonate to neutralize acidic impurities to provide an emulsion. About 150 mL of ethyl acetate was added to the emulsion to provide two phases. The aqueous phase was discarded and the organic phase washed with saturated Brine and dried over anhydrous sodium sulfate. The solvent was the removed under reduced pressure to provide tyrosine octanoate as a white solid that was purified using a silica gel column eluted with a 1:9 methanol:dichloromethane mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08017159B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-d7d1a7278f3f47b38428a75fe3dc3c9a |
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| Source note | uspto-grants-2011_09 |
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