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Acetic Acid → HCID 57875608, Verbindung

HRID 575930
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 575930
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([OH:10])=[C:6]([CH:9]=1)[CH:7]=O.[C:11]([O:15][C:16](=[O:19])[NH:17][NH2:18])([CH3:14])([CH3:13])[CH3:12].C(O)(=O)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl>[C:11]([O:15][C:16]([NH:17][NH:18][CH2:7][C:6]1[CH:9]=[C:2]([Br:1])[CH:3]=[CH:4][C:5]=1[OH:10])=[O:19])([CH3:14])([CH3:13])[CH3:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 176Acetic AcidHCID 70091tert-Butyl carbazateHCID 728635-BromosalicylaldehydeHCID 5049666Sodium triacetoxyborohydride

Produkt 1

HCID 57875608HCID 57875608, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344Dichloromethane
Lösungsmittel

Versuchsvorschrift

A solution of 5-bromo-2-hydroxybenzaldehyde (10 g g 50 mmol), tert-butylcarbazate (6.7 g, 52 mmol) and acetic acid (3 mL, 52 mmol) in CH2Cl2 (200 mL) was stirred under N2 atmosphere for 60 min at RT. Then sodium triacetoxyborohydride (34 g, 159 mmol) was added portion wise and the resulting mixture was stirred at RT overnight. The reaction was quenched with 2 M HCl (100 mL) and stirred at RT for 1 h. The reaction mixture was partitioned between water (100 mL) and CH2Cl2 (250 mL). The organic layer was washed with sat. NaHCO3 and brine (100 mL each), dried (MgSO4) and evaporated to dryness to give hydrazine 1 as a white solid, 13 g (82%).

Aufarbeitung

  1. customThe reaction was quenched with 2 M HCl (100 mL)
  2. stirringstirred at RT for 1 h
  3. customThe reaction mixture was partitioned between water (100 mL) and CH2Cl2 (250 mL)
  4. washThe organic layer was washed with sat. NaHCO3 and brine (100 mL each)
  5. dry with materialdried (MgSO4)
  6. customevaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-545292e06af7453b9990665695771074
Quelldatensatz
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09035071B2

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