2-Methylbenzoic acid → Mepronil

HRID 1287699

Reaktionsgleichung

Reaktionsgleichung von HRID 1287699
[CH3:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH:11]([O:14][C:15]1[CH:16]=[C:17]([CH:19]=[CH:20][CH:21]=1)[NH2:18])([CH3:13])[CH3:12].C(N(CC)CC)C.P(Cl)(Cl)(Cl)=O>C1(C)C(C)=CC=CC=1>[CH:11]([O:14][C:15]1[CH:16]=[C:17]([CH:19]=[CH:20][CH:21]=1)[NH:18][C:4](=[O:6])[C:3]1[CH:7]=[CH:8][CH:9]=[CH:10][C:2]=1[CH3:1])([CH3:13])[CH3:12]

Komponenten

6

Edukt 4

HCID 83732-Methylbenzoic acidHCID 8471TriethylamineHCID 24813Phosphorus oxychlorideHCID 5732203-Isopropoxyaniline

Produkt 1

HCID 41632MepronilAusbeute 77,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7237O-XyleneLösungsmittel

Versuchsvorschrift

A 13.6 g (0.1 mol) portion of o-methylbenzoic acid, 15.1 g (0.1 mol) of m-isopropoxyaniline and 10.1 g (0.1 mol) of triethylamine were dissolved in 100 ml of xylene. A 5.1 g (0.033 mol) amount of phosphorus oxychloride was added dropwise to the prepared solution with stirring at 90° - 100° C. Stirring of the resulting solution was continued at 90° - 100° C for 3 hours. The reaction mixture was cooled and washed with water, and the product was dried over anhydrous sodium sulfate. The xylene was removed to obtain 20.9 g (77.9%) of white prismatic crystals having a melting point of 92°-94° C.

Aufarbeitung

  1. stirringStirring of the resulting solution
  2. temperatureThe reaction mixture was cooled
  3. washwashed with water
  4. dry with materialthe product was dried over anhydrous sodium sulfate
  5. customThe xylene was removed

Quellen und Nachweise

ORD-Eintrag
ord-047315b6dd9645c3a248bc4d168187fd
Quelldatensatz
uspto-grants-1976_10
Patentnummer
US03985804

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