Benzoic acid, 2,6-dinitro- → Methyl 2,6-dinitrobenzoate

HRID 1076987

Reaktionsgleichung

Reaktionsgleichung von HRID 1076987
[N+:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[C:5]=1[C:6]([OH:8])=[O:7])([O-:3])=[O:2].[CH3:16]N1C=CCN(C2C=CC(C)=CC=2)N1>CCOCC>[N+:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]([N+:13]([O-:15])=[O:14])[C:5]=1[C:6]([O:8][CH3:16])=[O:7])([O-:3])=[O:2]

Komponenten

4

Edukt 2

HCID 119206Benzoic acid, 2,6-dinitro-HCID 202618531-Methyl-3-p-tolyltriazine

Produkt 1

HCID 333850Methyl 2,6-dinitrobenzoateAusbeute 37,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel2×

Versuchsvorschrift

2,6-Dinitrobenzoic acid (10.6 grams) is suspended in ether (125 ml.) at 0°C. 1-Methyl-3-p-tolyltriazine (8.2 grams) in ether (75 ml.) is added dropwise to the stirred reaction mixture in an ice bath. The reaction mixture is stirred at 0° for 1 hour and at room temperature for 1 hour. The reaction mixture is diluted to 1 l. with ether and the insoluble product collected by filtration. Recrystallization from methanol gives colorless crystals (3.65 grams, melting point 150°-151.5°). An additional 4.1 grams of product are obtained from the filtrate.

Aufarbeitung

  1. additionThe reaction mixture is diluted to 1 l
  2. filtrationwith ether and the insoluble product collected by filtration
  3. customRecrystallization from methanol

Quellen und Nachweise

ORD-Eintrag
ord-49f47bae1e5e4f5d8346bbff5a856aec
Quelldatensatz
uspto-grants-1976_05
Patentnummer
US03959289

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