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Acetic Acid → HCID 13257633, Verbindung

HRID 647403
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 647403
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:16](=[O:17])[C:15]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:9]2=[O:18])=[C:4]([F:19])[CH:3]=1.[BH4-].[Na+].C(O)(=O)C>C(O)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:16]([OH:17])[C:15]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:9]2=[O:18])=[C:4]([F:19])[CH:3]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 176Acetic AcidHCID 1859312-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dioneHCID 4311764Sodium borohydride

Produkt 1

HCID 13257633HCID 13257633, VerbindungAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

In 400 ml of ethanol was dissolved 40.0 g of 2-(4-chloro-2-fluorophenyl)-2,3,4,5,6,7-hexahydro-1H-isoindol-1,3-dione, and 2.4 g of sodium borohydride was added to the solution with stirring over a 30-minute period, while cooling was effected suitably to maintain the reaction temperature at 20° to 30° C. After stirring was continued at room temperature for one hour, the reaction mixture was neutralized with dilute acetic acid and concentrated to about one third of the original volume. Upon cooling, there resulted crystals, which were collected by filtration, washed with water and dried, thereby affording 36.2 g (yield of 90%) of the subject compound. Recrystallization from ethyl acetate yielded white crystals, m.p. 178°-179° C.

Aufarbeitung

  1. additionwas added to the solution
  2. temperaturewhile cooling
  3. temperatureto maintain the reaction temperature at 20° to 30° C
  4. stirringAfter stirring
  5. concentrationconcentrated to about one third of the original volume
  6. temperatureUpon cooling
  7. customthere resulted crystals, which
  8. filtrationwere collected by filtration
  9. washwashed with water
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-c35e4c79845c4ccbb76e9d7e609446bb
Quelldatensatz
uspto-grants-1983_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04409018

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