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Hydrochloric Acid → 4-Chloro-2,3-dihydro-1H-isoindole

HRID 1630
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1630
Cl[C:2]1[CH:3]=[C:4]2[C:9](=O)[NH:8][C:6](=O)[C:5]2=[CH:11][CH:12]=1.[ClH:13]>O1CCCC1>[Cl:13][C:11]1[CH:12]=[CH:2][CH:3]=[C:4]2[C:5]=1[CH2:6][NH:8][CH2:9]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 2312394-Chloro-phthalimide

Produkt 1

HCID 147958684-Chloro-2,3-dihydro-1H-isoindole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a solution of 4-chlorophthalimide (60 g) in 1 liter of tetrahydrofuran was added borane-methyl sulfide complex (100 ml of 10M), and the mixture was refluxed overnight. After cooling, 100 ml of 6N hydrochloric acid was added slowly, the mixture refluxed for 2 hours, and then filtered. The filtrate was concentrated under reduced pressure, and the resulting aqueous solution washed with ethyl acetate. The aqueous layer was then basified with ammonium hydroxide and extracted with methylene chloride. Solvent was removed from the extract, and the residue distilled under vacuum to give 4-chloroisoindoline, a white solid, m.p. 48°-50° C.

Aufarbeitung

  1. temperaturethe mixture was refluxed overnight
  2. temperatureAfter cooling
  3. temperaturethe mixture refluxed for 2 hours
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. washthe resulting aqueous solution washed with ethyl acetate
  7. extractionextracted with methylene chloride
  8. customSolvent was removed from the extract
  9. distillationthe residue distilled under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-9c7cc9bbc71144c7ae9f1e2d0e680324
Quelldatensatz
uspto-grants-1998_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05726197

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