Triethylamine → O,O-diethyl isopropyl[[(fluorocarbonyl)methylamino]thio]phosphoramidothioate

HRID 2295380

Reaktionsgleichung

Reaktionsgleichung von HRID 2295380
[CH:1]([NH:4][P:5](=[S:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8])([CH3:3])[CH3:2].C([N:15]([CH2:18]C)CC)C.ClSN(C)[C:23]([F:25])=[O:24].ON=C([S:31]C)C>O1CCCC1.CCOCC>[CH:1]([N:4]([S:31][NH:15][CH2:18][C:23]([F:25])=[O:24])[P:5](=[S:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8])([CH3:3])[CH3:2]

Komponenten

7

Versuchsvorschrift

A solution of O,O-diethyl isopropylphosphoramidothioate (14.9 g, 70.8 mmol) and triethylamine (9.8 ml, 70.8 mmol) in tetrahydrofuran (50 ml) is added dropwise over 10 minutes to a solution of N-chlorothio(methyl)carbamoyl fluoride (10.2 g, 70.8 mmol) in tetrahydrofuran (50 ml) cooled in an ice bath. After the addition the mixture is stirred for 1.5 hours at 0°, diluted with ether (200 ml), washed with ice cold water, dried over sodium sulfate and concentrated under reduced pressure. The residue shows identical absorptions in the ir and pmr spectra for γ C=O and N--CH3 as obtained for the yellow oil that is intermediate II1 of Example 1. The crude II1 product is suitable for reaction with methyl N-hydroxyethanimidothioate as in Example 1.

Aufarbeitung

  1. temperaturecooled in an ice bath
  2. additionAfter the addition the mixture
  3. washwashed with ice cold water
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. customas obtained for the yellow oil that

Quellen und Nachweise

ORD-Eintrag
ord-d166b7e57f0d4204aee89cbe332ceaae
Quelldatensatz
uspto-grants-1984_01
Patentnummer
US04424368

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