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Hydrochloric Acid → 4-Bromo-1-chloro-3-methylbenzaldoxime

HRID 452517
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 452517
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([CH:6]=[N:7][OH:8])=[CH:4][C:3]=1[CH3:11].[ClH:12].Cl[O-].[Na+]>O1CCCC1>[Br:1][C:2]1[CH:10]=[CH:9][C:5]([Cl:12])([CH:6]=[N:7][OH:8])[CH2:4][C:3]=1[CH3:11]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 23665760Sodium HypochloriteHCID 738479544-Bromo-3-methylbenzaldehyde oxime

Produkt 1

HCID 866675374-Bromo-1-chloro-3-methylbenzaldoximeAusbeute 97,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

In a solution of 82.0 g of 4-bromo-3-methylbenzaldoxime in 450 ml of tetrahydrofuran, 120.0 g of concentrated hydrochloric acid was added adropwise with stirring under ice cooling over 45 minutes. Then, 220 ml of 8% sodium hypochlorite aqueous solution was carefully added dropwise over 75 minutes so that the temperature of the reaction mixture would not exceed 5° C., after the completion of the addition, continued to stir at 10° C. or less further for 90 minutes. After the completion of the reaction, nitrogen gas was blown through the reaction mixture for 45 minutes and precipitated insoluble material was filtered off, and tetrahydrofuran was distilled off under reduced pressure. The remaining aqueous solution was extracted with 240.0 g of ethyl acetate. The organic phase was washed with water (240 ml×2) and then insoluble material was filtered off, the solvent was distilled off under reduced pressure to obtain 93.5 g of the aimed product as pale yellow crystal.

Aufarbeitung

  1. customexceed 5° C.
  2. additionafter the completion of the addition
  3. stirringto stir at 10° C. or less further for 90 minutes
  4. customAfter the completion of the reaction, nitrogen gas
  5. waitwas blown through the reaction mixture for 45 minutes
  6. customprecipitated insoluble material
  7. filtrationwas filtered off
  8. distillationtetrahydrofuran was distilled off under reduced pressure
  9. extractionThe remaining aqueous solution was extracted with 240.0 g of ethyl acetate
  10. washThe organic phase was washed with water (240 ml×2)
  11. filtrationinsoluble material was filtered off
  12. distillationthe solvent was distilled off under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-110b60a2859845b8aa1d76e2aba639bb
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08492311B2

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