HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54862Erstellt: 25. Oktober 2026
Hydrochloric Acid → N-[(2-Adamantyloxy)carbonyl]-alpha-trimethylsilylethoxymethyl-DL-tryptophan
https://huagongshe.com/reaction/54862
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | N-[(2-Adamantyloxy)carbonyl]-alpha-trimethylsilylethoxymethyl-DL-tryptophan methyl ester | HCID 86747503 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | N-[(2-Adamantyloxy)carbonyl]-alpha-trimethylsilylethoxymethyl-DL-tryptophan | HCID 86747505 | 91,8% |
Reaktionsschritte
A mixture of N-[(2-adamantyloxy)carbonyl]-α-trimethylsilylethoxymethyl-DL-tryptophan methyl ester (4.5 g, 8.5 mmol), LiOH (0.22 g, 9.1 mmol), dioxane (90 mL), and water (30 mL) was stirred at 60° C. for 16 hours. After cooling, the reaction mixture was acidified to pH 4 with 1N hydrochloric acid and extracted with ethyl acetate. The organic extract was dried over Na2SO4 and then concentrated in vacuo. Trituration of the oily residue with diethyl ether gave the title compound as a white solid (4.0 g, 91.7%), mp 203° C. (dec.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05622983 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-8f462b831ee44228862923ab80b54353 |
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| Quellennotiz | uspto-grants-1997_04 |
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