4-Hydroxybenzamide → Ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate

HRID 484364

Reaktionsgleichung

Reaktionsgleichung von HRID 484364
[CH3:1][C:2]1([CH3:26])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14]([O:16][C:17]3[CH:25]=[CH:24][C:20]([C:21](N)=[O:22])=[CH:19][CH:18]=3)=[O:15])[CH:5]=[CH:4][C:3]1=2.[OH:27][C:28]1C=CC(C(N)=O)=C[CH:29]=1>>[CH3:1][C:2]1([CH3:26])[CH2:11][CH2:10][C:9]([CH3:13])([CH3:12])[C:8]2[CH:7]=[C:6]([C:14]([O:16][C:17]3[CH:25]=[CH:24][C:20]([C:21]([O:27][CH2:28][CH3:29])=[O:22])=[CH:19][CH:18]=3)=[O:15])[CH:5]=[CH:4][C:3]1=2

Komponenten

3

Edukt 2

HCID 650524-HydroxybenzamideHCID 197480184-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzamide

Produkt 1

HCID 19748015Ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate

Versuchsvorschrift

4-(5,5,8,8-Tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzamide-Using 4-hydroxybenzamide, the title compound was synthesized as a white solid. PMR (CDCl3): δ 1.35 (6H, s), 1.37 (6H, s), 1.76 (4H, s), 7.32 (2H, d, J~8.6 Hz), 7.48 (1H, d, J~8.4 Hz), 7.89-7.98 (3H, m), 8.17 (1H, d, J~1.9 Hz).

Quellen und Nachweise

ORD-Eintrag
ord-8698c61e71b84a9da03c69b9d478a7ca
Quelldatensatz
uspto-grants-1993_07
Patentnummer
US05231113

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