Propoxur → 2-Isopropoxyphenyl [[(diethoxyphosphinothioyl)anilino]thio]methylcarbamate

HRID 1706708

Reaktionsgleichung

Reaktionsgleichung von HRID 1706708
Cl[S:2][N:3]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[P:4](=[S:11])([O:8][CH2:9][CH3:10])[O:5][CH2:6][CH3:7].[CH3:18][NH:19][C:20](=[O:32])[O:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[O:28][CH:29]([CH3:31])[CH3:30].CN(C)C=O>C(OCC)C.O>[CH2:6]([O:5][P:4]([N:3]([S:2][CH2:18][NH:19][C:20](=[O:32])[O:21][C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=1[O:28][CH:29]([CH3:30])[CH3:31])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)([O:8][CH2:9][CH3:10])=[S:11])[CH3:7]

Komponenten

6

Edukt 3

HCID 4944PropoxurHCID 6228DimethylformamideHCID 54509702O,O-diethyl N-(chlorothio)phenylphosphoramidothioate

Produkt 1

HCID 203412672-Isopropoxyphenyl [[(diethoxyphosphinothioyl)anilino]thio]methylcarbamate

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 3283Diethyl EtherLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

The O,O-diethyl N-(chlorothio)phenylphosphoramidothioate as a yellow oil obtained in Part A, above, is dissolved in a minimal amount of diethyl ether (about 5 ml) and the ether solution is added to a cooled (0° C.) solution consisting of 6.34 gm (0.030 mole) of 2-isopropoxyphenyl methylcarbamate and 20 ml dimethylformamide. This reaction mixture is stirred as it is permitted to warm to 25° C., and stirring is continued for four hours. The mixture is then diluted with 100 ml water and extracted with diethyl ether. The ether phase is recovered, washed with water, and dried over anhydrous sodium sulfate. The ether is removed by evaporation under reduced pressure. The oily residue thus obtained is chromatographed through a column of silica gel. Development is with methylene chloride. After removing the methylene chloride by evaporation under reduced pressure, there is obtained 1.02 gm. of the crude product as an amber oil which is crystallized from petroleum ether having a boiling range between 30° and 60° C. to give 2-isopropoxyphenyl [[(diethoxyphosphinothioyl)anilino]thio]methylcarbamate as colorless crystals having a melting point at 69° to 70.5° C.

Aufarbeitung

  1. temperatureto warm to 25° C.
  2. stirringstirring
  3. extractionextracted with diethyl ether
  4. customThe ether phase is recovered
  5. washwashed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. customThe ether is removed by evaporation under reduced pressure
  8. customThe oily residue thus obtained
  9. customis chromatographed through a column of silica gel
  10. customAfter removing the methylene chloride
  11. customby evaporation under reduced pressure
  12. customthere is obtained 1.02 gm
  13. customof the crude product as an amber oil which is crystallized from petroleum ether having a boiling range between 30° and 60° C.

Quellen und Nachweise

ORD-Eintrag
ord-4f29e5e05eff4e3fa292484e506433ac
Quelldatensatz
uspto-grants-1980_06
Patentnummer
US04208409

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