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Hydrochloric Acid → HCID 178463117, Verbindung

HRID 369578
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 369578
[Cl:1][C:2]1[C:10]([Cl:11])=[C:9]([S:12]([CH3:15])(=[O:14])=[O:13])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=O.[CH2:16]([N:18]1[C:22]([OH:23])=[CH:21][CH:20]=[N:19]1)[CH3:17].C1(N=C=NC2CCCCC2)CCCCC1.Cl>C(#N)C>[CH2:16]([N:18]1[C:22]([OH:23])=[C:21]([C:4](=[O:6])[C:3]2[CH:7]=[CH:8][C:9]([S:12]([CH3:15])(=[O:14])=[O:13])=[C:10]([Cl:11])[C:2]=2[Cl:1])[CH:20]=[N:19]1)[CH3:17]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 313Hydrochloric AcidHCID 10868DicyclohexylcarbodiimideHCID 27869432,3-Dichloro-4-methylsulfonylbenzoic acidHCID 178418331HCID 178418331, Verbindung

Produkt 1

HCID 178463117HCID 178463117, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342
Acetonitrile
Lösungsmittel

Versuchsvorschrift

A solution of 500 mg (1.85 mmol) of 2,3-dichloro-4-methylsulfonylbenzoic acid and 240 mg (2.14 mmol) of 1-ethyl-5-hydroxypyrazole in 10 mL of dry acetonitrile was treated with 430 mg (2.08 mmol) of dicyclohexylcarbodiimide with stirring at ambient temperature for 0.5 hr. The precipitate that formed was removed by filtration and the filtrate was treated with 0.5 mL of triethylamine and 1 mL of acetone cyanohydrin. After 1 hr, the reaction mixture was partitioned between dichloromethane and 1N aqueous hydrochloric acid. The organic layer was recovered and extracted with dilute aqueous sodium bicarbonate solution. The basic aqueous solution obtained was acidified with dilute aqueous hydrochloric acid and extracted with dichloromethane. The organic extract was dried over sodium sulfate and concentrated by evaporation under reduced pressure to obtain 540 mg (81 percent of theory )of the title compound as an orange syrup.

Aufarbeitung

  1. customThe precipitate that formed
  2. customwas removed by filtration
  3. additionthe filtrate was treated with 0.5 mL of triethylamine and 1 mL of acetone cyanohydrin
  4. waitAfter 1 hr
  5. customthe reaction mixture was partitioned between dichloromethane and 1N aqueous hydrochloric acid
  6. customThe organic layer was recovered
  7. extractionextracted with dilute aqueous sodium bicarbonate solution
  8. customThe basic aqueous solution obtained
  9. extractionextracted with dichloromethane
  10. extractionThe organic extract
  11. dry with materialwas dried over sodium sulfate
  12. concentrationconcentrated by evaporation under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-73e1010db1744d81ab984eebb84b1286
Quelldatensatz
uspto-grants-2000_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06140271

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