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

HRID 21670

Reaktionsgleichung

Reaktionsgleichung von HRID 21670
[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-9570592e9f8441c1bc76aa768282e77a
Quelldatensatz
uspto-grants-1995_06
Patentnummer
US05424333

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