4H-1-Benzopyran-2-carboxylic acid, 4-oxo-, methyl ester → Methyl 3,4-dihydro-2H-1-benzopyran-2-carboxylate
Reaktionsgleichung
O=[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5][C:4]([C:12]([O:14][CH3:15])=[O:13])=[CH:3]1.COC(C1CCC2C(=CC=C(S(Cl)(=O)=O)C=2)O1)=O>[Pd]>[CH3:15][O:14][C:12]([CH:4]1[CH2:3][CH2:2][C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[O:5]1)=[O:13]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Compound 3A was prepared by hydrogenation of the methyl 4-oxo-4H-chromene-2-carboxylate catalyzed by 10% Pd/C in 93% yield. MS: MS: 193 (M+1)+. Preparation of 6-Chlorosulfonyl-chroman-2-carboxylic acid methyl ester (Compound 3B)
Quellen und Nachweise
- ORD-Eintrag
- ord-5eb2bf08cb4a45bc9e728fd87e6b006c
- Quelldatensatz
- uspto-grants-2005_03
- Patentnummer
- US06867224B2
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