HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429913Erstellt: 23. Oktober 2026
Sulfuric Acid → tert-butyl (2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoate
https://huagongshe.com/de/reaction/429913
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Isobutylene | HCID 8255 | — |
| Edukt | 3-Iodo-L-Tyrosine | HCID 439744 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | tert-butyl (2S)-2-amino-3-(4-hydroxy-3-iodophenyl)propanoate | HCID 57291941 | 58% |
Reaktionsschritte
A mixture of 5.0 g of 3-iodo-L-tyrosine (Aldrich) and 2.5 mL of conc. H2SO4 in 85 mL of 1,4-dioxane was added to 30 mL of liquid isobutylene (condensed at −78° C.) in a 300 mL pressure bottle. The vessel was stoppered and the contents stirred at RT. After 3 days the bottle was cooled in an ice water bath, opened and the solution poured into a mixture of 10 g of NaHCO3 in 150 mL of water. The resulting mixture was subjected to rotary evaporation to remove isobutylene and dioxane. A white solid resulted which was collected by filtration and dried in vacuo. Analysis by tlc (SiO2, 95:5 CH2Cl2:MeOH) indicated major and minor components at Rf=0.52 and 0.60 respectively. The crude product was purified by flash chromatography on silica gel (95:5 CH2Cl2:MeOH) to afford 3.4 g (58%) of tert-butyl 3-iodo-L-tyrosinate as a white crystalline solid, m.p. 158-159° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06319702B1 |
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| Quelldatensatz | uspto-grants-2001_11 |
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| ORD ID | ord-5fb542aab96648f592defa820e5599a9 |
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| Quellennotiz | uspto-grants-2001_11 |
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