Diethyl Ether → N'-t-butyl-N'-[methyl-(2-chlorophenylamino)phosphinyl]-N-benzoylhydrazine

HRID 849799

Reaktionsgleichung

Reaktionsgleichung von HRID 849799
[CH3:1][P:2](Cl)Cl.[C:5]([NH:13][NH:14][C:15]([CH3:18])([CH3:17])[CH3:16])(=[O:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[Cl:19][C:20]1[CH:26]=[CH:25][CH:24]=[CH:23][C:21]=1[NH2:22].CC[O:29]CC>C(N(CC)CC)C.C(Cl)Cl>[C:15]([N:14]([P:2]([CH3:1])([NH:22][C:21]1[CH:23]=[CH:24][CH:25]=[CH:26][C:20]=1[Cl:19])=[O:29])[NH:13][C:5](=[O:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1)([CH3:18])([CH3:17])[CH3:16]

Komponenten

7

Versuchsvorschrift

Methyl dichlorophosphine (1.3 g) in ether (10 ml) and triethylamine (2 ml) were added to a stirred solution of N-benzoyl-N'-t-butyl hydrazine (1.0 g) in methylene chloride (3 ml). After stirring 5 minutes at room temperature, o-chloroaniline was added neat producing a mild exotherm. The reaction was quenched 2 minutes later with water (20 ml) and ether (20 ml), separated and the organic washed with 0.1N HCl, dried over MgSO4, filtered and rotavapped to a colorless oil weighing 0.5 g.

Aufarbeitung

  1. customproducing a mild exotherm
  2. customThe reaction was quenched 2 minutes later with water (20 ml) and ether (20 ml)
  3. customseparated
  4. washthe organic washed with 0.1N HCl
  5. dry with materialdried over MgSO4
  6. filtrationfiltered

Quellen und Nachweise

ORD-Eintrag
ord-622f237a76ee4662ac826ca1c7dcdf06
Quelldatensatz
uspto-grants-2000_01
Patentnummer
US06013836

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