HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 629668Erstellt: 24. Oktober 2026
Di-tert-butyl glutamate hydrochloride → HCID 68695638, Verbindung
https://huagongshe.com/de/reaction/629668
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Di-tert-butyl glutamate hydrochloride | HCID 208636 | — |
| Edukt | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Edukt | HCID 21951876 | HCID 21951876 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 68695638 | HCID 68695638 | — |
Reaktionsschritte
To a mixture of 4-(tert-butoxycarbonylamino)-2-nitrobenzoic acid in 60 ml of dichloromethane were added 4.8 g of N,N,N′,N′-tetramethyl-O-(1H-benzotriazol-1-yl)-uronium-hexafluorophosphate. After stirring for 15 min. a mixture of 3.8 g of L-glutamic acid-di tert.-butylester hydrochloride in 60 ml dichloromethane and 3 ml triethylamine was added dropwise. After stirring for 20 hours at room temperature, the mixture was filtered and the filtrate was washed five times with 10% aqueous citric acid, four times with 5% aqueous sodium carbonate solution and two times with water. The organic layer was dried over magnesium sulphate and concentrated in vacuum to give 6.3 g of di-tert-butyl N-(4-(tert-butoxycarbonylamino)-2-nitrobenzamido)-L-glutamate as a yellow foam. This was directly used in example 3.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09315506B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-5050c73064234dc0801cc0c6f60729b4 |
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| Quellennotiz | uspto-grants-2016_04 |
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