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Hydrochloric Acid → HCID 86693072, Verbindung

HRID 575040
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 575040
[Br:1][C:2]1[CH:12]=[C:11]2[C:5]([CH:6]3[CH2:20][CH:8]([N:9]=[C:10]2[NH:13][CH2:14][CH:15](OC)OC)[CH2:7]3)=[CH:4][CH:3]=1.Cl>O1CCCC1>[Br:1][C:2]1[CH:12]=[C:11]2[C:5](=[CH:4][CH:3]=1)[CH:6]1[CH2:20][CH:8]([CH2:7]1)[N:9]1[C:10]2=[N:13][CH:14]=[CH:15]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 313Hydrochloric AcidHCID 178495871HCID 178495871, Verbindung

Produkt 1

HCID 86693072HCID 86693072, VerbindungAusbeute 55,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Into a 1000-mL round-bottom flask was placed 5-bromo-N-(2,2-dimethoxyethyl)-9-azatricyclo[8.1.1.0[2,7]]dodeca-2,4,6,8-tetraen-8-amine (33.4 g, 98.46 mmol, 1.00 equiv), tetrahydrofuran (340 mL), and hydrogen chloride (340 mL, 10%). The resulting solution was heated to reflux for 2 h, concentrated under vacuum and extracted with 2×150 mL of ethyl acetate. The pH value of the combined aqueous layers was adjusted to 8-9 with sodium hydroxide (2 mol/L). The resulting solution was extracted with 3×300 mL of dichloromethane. The organic layers were combined, washed with 2×150 mL of water and 1×150 mL of brine, dried over anhydrous sodium sulfated and concentrated under vacuum. The crude product was decolorized by the addition of active carbon, stirring for 30 min. The solids were filtered out and the filtrate was concentrated under vacuum to afford 15 g (55%) of 9-bromo-2,5-diazatetracyclo[11.1.1.0[2,6].0[7,12]]pentadeca-3,5,7,9,11-pentaene as a white solid.

Aufarbeitung

  1. customInto a 1000-mL round-bottom flask was placed
  2. temperatureThe resulting solution was heated
  3. temperatureto reflux for 2 h
  4. concentrationconcentrated under vacuum
  5. extractionextracted with 2×150 mL of ethyl acetate
  6. extractionThe resulting solution was extracted with 3×300 mL of dichloromethane
  7. washwashed with 2×150 mL of water and 1×150 mL of brine
  8. dry with materialdried over anhydrous sodium
  9. concentrationconcentrated under vacuum
  10. additionThe crude product was decolorized by the addition of active carbon
  11. filtrationThe solids were filtered out
  12. concentrationthe filtrate was concentrated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-7dadd9b58bc245bea9de99da06acd882
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09034866B2

Notizen zur Reaktion

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