Nitric Acid → Benzoic acid, 3,5-bis(1,1-dimethylethyl)-2-nitro-

HRID 52795

Reaktionsgleichung

Reaktionsgleichung von HRID 52795
[C:1]([C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([C:14]([CH3:17])([CH3:16])[CH3:15])[CH:13]=1)[C:8]([OH:10])=[O:9])([CH3:4])([CH3:3])[CH3:2].[N+:18]([O-:21])([OH:20])=[O:19].S(Cl)([Cl:24])=O>CN(C)C=O>[C:1]([C:5]1[C:6]([N+:18]([O-:21])=[O:19])=[C:7]([CH:11]=[C:12]([C:14]([CH3:17])([CH3:16])[CH3:15])[CH:13]=1)[C:8]([Cl:24])=[O:9])([CH3:4])([CH3:3])[CH3:2].[C:1]([C:5]1[C:6]([N+:18]([O-:20])=[O:19])=[C:7]([CH:11]=[C:12]([C:14]([CH3:17])([CH3:16])[CH3:15])[CH:13]=1)[C:8]([OH:10])=[O:9])([CH3:4])([CH3:3])[CH3:2]

Komponenten

6

Versuchsvorschrift

3,5-Di-t-butyl-2-nitrobenzoyl chloride was prepared by nitration of 3,5-di-t-butylbenzoic acid 46.86 grams (0.20 mol) with 90% nitric acid (150 ml, d=1.5) to give 3,5-di-t-butyl-2-nitrobenzoic acid (54.6 grams) followedby treatment with thionyl chloride (250 ml) with dimethylformamide (1 ml).

Quellen und Nachweise

ORD-Eintrag
ord-1b0b73807bcb47e7ad054cd94bc82b55
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05616797

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