Potassium Hydroxide → [4-(Diazo(phenyl)methyl)phenyl]methanol

HRID 40451

Reaktionsgleichung

Reaktionsgleichung von HRID 40451
S([O-])([O-])(=O)=O.[Na+].[Na+].[OH-].[K+].[OH:10][CH2:11][C:12]1[CH:26]=[CH:25][C:15]([C:16](=[N:23][NH2:24])[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[CH:14][CH:13]=1>C(O)C.C1COCC1.[Hg]=O>[N+:23](=[C:16]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[C:15]1[CH:14]=[CH:13][C:12]([CH2:11][OH:10])=[CH:26][CH:25]=1)=[N-:24]

Komponenten

7

Edukt 3

HCID 14797Potassium HydroxideHCID 24436Sodium SulfateHCID 722408194-Hydroxymethyl benzophenone hydrazone

Produkt 1

HCID 86639975[4-(Diazo(phenyl)methyl)phenyl]methanolAusbeute 100 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 30856Mercuric oxideKatalysatorHCID 702EthanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a mixture of mercury (II) oxide (2.9 g, 13 mmol), sodium sulphate (2.2 g, 15 mmol) and sat potassium hydroxide in ethanol (4 ml) was added a solution of 4 (2.6 g, 11 mmol) in dry THF (20 ml). The mixture was stirred in the dark for 2 h. then filtered through a celite pad. Concentration of the filtrate in vacuo yielded 5 (2.4 g, 100%) as a dark red oil; δH (CDCl3) 4.69 (s, 2H, CH2OH), 7.29-7.31 (m, 4H, 3-, 3′-, 5-, 5′-H), 7.39-7.41 (m, 5H, 2-, 2′-, 4′-, 6-, 6′-H) ppm; δC (CDCl3) 64.8 (CH2OH), 125.1, 125.2 (3-, 3′-, 5-, 5′-C), 125.6 (4′-C), 127.9, 129.1 (2-, 2′-, 6-, 6′-C), 128.9, 129.4 (1-, 1′-C), 138.2 (4-C) ppm; νmax (thin film) 3346, 2872, 2038, 1511, 1493 cm−1; m/z (F14) 224 ([M]+, 100%); found (FT) 224.0949, C14H12N2O requires 224.0950.

Aufarbeitung

  1. filtrationthen filtered through a celite pad

Quellen und Nachweise

ORD-Eintrag
ord-a3077c37d0144660b1f75c90b50b330f
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08530212B2

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