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Dimethylformamide → 2-Chloro-5-nitrobenzo[d]oxazole

HRID 512450
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 512450
S[C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=2[N:6]=1.CN(C=O)C.S(Cl)([Cl:21])=O>>[Cl:21][C:2]1[O:3][C:4]2[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=2[N:6]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 178526504HCID 178526504, Verbindung

Produkt 1

HCID 103527232-Chloro-5-nitrobenzo[d]oxazole

Reaktionsbedingungen

Temperatur
65 °C

Versuchsvorschrift

Subsequently, the crude 2-mercapto-5-nitrobenzoxazole (10 g, 51 mmol), previously prepared, was dissolved in thionyl chloride (100 mL). DMF (60 μL) was added and the reaction mixture was heated at 65° C. for 45 min. After cooling, the solvent was removed under reduced pressure and to the residue, toluene was added twice (2×20 mL) and each time subsequently evaporated in vacuo to remove volatiles via azeotrope. The resultant crude product was dissolved in ethyl acetate (400 mL), washed with brine (200 mL), dried over Na2SO4, filtered, and concentrated to give compound 29, 2-chloro-5-nitrobenzoxazole, as (8.2 g, crude).

Aufarbeitung

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure and to the residue, toluene
  3. additionwas added twice (2×20 mL)
  4. customeach time subsequently evaporated in vacuo
  5. customto remove volatiles via azeotrope
  6. dissolutionThe resultant crude product was dissolved in ethyl acetate (400 mL)
  7. washwashed with brine (200 mL)
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-a8933e70a14844059ac74a47cc63921b
Quelldatensatz
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09102636B2

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