2-Methylbenzoic acid → N-(3-Methoxyphenyl)-2-methylbenzene-1-carboximidic acid

HRID 1287697Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1287697
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH2:16].C(N(CC)CC)C.P(Cl)(Cl)Cl>C1(C)C=CC=CC=1>[CH3:11][O:12][C:13]1[CH:14]=[C:15]([CH:17]=[CH:18][CH:19]=1)[NH:16][C:4](=[O:6])[C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=1[CH3:1]

Komponenten

6

Edukt 4

HCID 83732-Methylbenzoic acidHCID 8471TriethylamineHCID 108243-MethoxyanilineHCID 24387Phosphorus trichloride

Produkt 1

HCID 185821N-(3-Methoxyphenyl)-2-methylbenzene-1-carboximidic acidAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

A 13.6 g (0.1 mol) portion of o-methylbenzoic acid, 10.9 g (0.1 mol) of m-methoxyaniline and 10.1 g (0.1 mol) of triethylamine were dissolved in 250 ml of toluene. A 4.6 g (0.033 mol) amount of phosphorus trichloride was added dropwise to the above solution with stirring at 20°-60° C. After the addition, the reaction mixture was stirred at 80°-90° C for 3 hours. The reaction mixture was cooled and washed with water to remove the triethylamine hydrochloride, and the product was dried over anhydrous sodium sulfate. The toluene was removed to give 22.8 g (95%) of fine white prismatic crystals having a melting point of 142°-143° C.

Aufarbeitung

  1. additionAfter the addition
  2. stirringthe reaction mixture was stirred at 80°-90° C for 3 hours
  3. temperatureThe reaction mixture was cooled
  4. washwashed with water
  5. customto remove the triethylamine hydrochloride
  6. dry with materialthe product was dried over anhydrous sodium sulfate
  7. customThe toluene was removed

Quellen und Nachweise

ORD-Eintrag
ord-f35820833f9244fd8702dc9f84149518
Quelldatensatz
uspto-grants-1976_10
Patentnummer
US03985804

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