HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 413402Erstellt: 25. Oktober 2026
N-(tert-butoxycarbonyl)glycine → N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl ester
https://huagongshe.com/reaction/413402
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | N-(tert-butoxycarbonyl)glycine | HCID 78288 | — |
| Edukt | cis-4-Benzyloxy-2-buten-1-ol | HCID 11008492 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-[(1,1-Dimethylethoxy)carbonyl]glycine-4phenylmethoxy-2-butenyl ester | HCID 69891095 | — |
Reaktionsschritte
N-[(1,1-Dimethylethoxy)carbonyl]glycine (21.9 grams, 0.125 mol), cis-4-benzyloxy-2-buten-1-ol (25 mL, 0.15 mol), and 4-dimethylaminopyridine (1.5 grams, 0.013 mol) are dissolved in methylene chloride and stirred at 0° C. Then N,N-dicyclohexylcarbodiimide (31 grams, 0.15 mol) in 30 mL methylene chloride is added and the reaction is stirred at 0° C. for five minutes. The reaction is then stirred for an additional twelve hours at 25° C. Additional methylene chloride is added and the reaction is washed consecutively with 1 N HCl, sodium bicarbonate and then with brine. The organic extract is dried over magnesium sulfate and the solvent evaporated in vacuo to give an orange oil which is absorbed onto silica gel and applied to a dry silica column. The column is eluted with hexane/EtOAc (9:1) then with hexane/EtOAc (8:2) Product fractions are combined and dried in vacuo to give the desired product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06566381B1 |
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| Quelldatensatz | uspto-grants-2003_05 |
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| ORD ID | ord-fc51b361b1384d3aa246311f51cb3677 |
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| Quellennotiz | uspto-grants-2003_05 |
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