Hydrochloric Acid → 2,3-Dihydro-1H-isoindol-5-ol--hydrogen chloride (1/1)
Reaktionsgleichung
[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH2:7][N:6](C(OC(C)(C)C)=O)[CH2:5]2.[ClH:18]>O1CCOCC1>[ClH:18].[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[CH2:7][NH:6][CH2:5]2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2 g (235.3 mmol) of tert-butyl 5-hydroxy-1,3-dihydroisoindole-2-carboxylate are dissolved in 20 ml of a 4 M hydrogen chloride solution in dioxane. After 1 h at 22° C., the mixture is evaporated to dryness in vacuo. The resultant white crystals (1.4 g (96%) MW 171.6) are employed in the following reactions without further purification.
Aufarbeitung
- customthe mixture is evaporated to dryness in vacuo
- customThe resultant white crystals (1.4 g (96%) MW 171.6) are employed in the following reactions without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-db4b9eefd42a4c47a3ca5625b5336577
- Quelldatensatz
- uspto-grants-2012_05
- Patentnummer
- US08183279B2
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