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Sodium borohydride → HCID 12096237, Verbindung

HRID 2185006
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2185006
[Br:1][C:2]1[C:10]2[S:9](=[O:12])(=[O:11])[N:8](C(C)(C)C)[CH:7](O)[C:6]=2[CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>C(O)=O>[Br:1][C:2]1[C:10]2[S:9](=[O:12])(=[O:11])[NH:8][CH2:7][C:6]=2[CH:5]=[CH:4][CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 4311764Sodium borohydrideHCID 12046097HCID 12046097, Verbindung

Produkt 1

HCID 12096237HCID 12096237, VerbindungAusbeute 60 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 284Formic AcidLösungsmittel

Versuchsvorschrift

7-bromo-2-(1,1-dimethylethyl)-2,3-dihydro-1,2-benzisothiazol-3-ol 1,1-dioxide (1.4 g, 4.4 mmol) was treated with formic acid (10 mL). The reaction was stirred at ambient temperature over 18 h, concentrated in vacuo and dissolved in methanol (10 mL). The mixture was cooled to 0° C. and treated with sodium borohydride (0.17 g, 4.4 mmol) in small portions over 20 min. The cooling bath was removed and the resulting reaction mixture stirred at ambient temperature over 18 h. The work-up consisted of slowly quenching the reaction mixture with ice, dilution with water and extraction with ethyl acetate. Drying over sodium sulfate and concentrating under reduced pressure provided the crude product that was purified by a plug of silica gel (ethyl acetate/hexane, 1:4) to afford the desired 7-bromo-2,3-dihydro-1,2-benzisothiazole 1,1-dioxide (0.6 g, 60% over 2 steps). 1H NMR (CD3OD): δ4.40 (s, 2H), 7.53 (m, 2H), 7.70 (m, 1H).

Aufarbeitung

  1. concentrationconcentrated in vacuo
  2. dissolutiondissolved in methanol (10 mL)
  3. temperatureThe mixture was cooled to 0° C.
  4. customThe cooling bath was removed
  5. customthe resulting reaction mixture
  6. stirringstirred at ambient temperature over 18 h
  7. customof slowly quenching the reaction mixture with ice, dilution
  8. extractionwith water and extraction with ethyl acetate
  9. dry with materialDrying over sodium sulfate
  10. concentrationconcentrating under reduced pressure
  11. customprovided the crude product that
  12. customwas purified by a plug of silica gel (ethyl acetate/hexane, 1:4)

Quellen und Nachweise

ORD-Eintrag
ord-77be1c13b1bd4664b608e2e029148d79
Quelldatensatz
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06399644B1

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