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Methanol → 5-Bromo-6-hydroxy-7-methyl-quinoline

HRID 931744
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 931744
[Br:1][C:2]1[C:11]([O:12]C)=[C:10]([CH3:14])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2.B(Br)(Br)Br.CO>C(Cl)Cl>[Br:1][C:2]1[C:11]([OH:12])=[C:10]([CH3:14])[CH:9]=[C:8]2[C:3]=1[CH:4]=[CH:5][CH:6]=[N:7]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 887MethanolHCID 25134Boron tribromideHCID 666307145-Bromo-6-methoxy-7-methylquinoline

Produkt 1

HCID 230783095-Bromo-6-hydroxy-7-methyl-quinolineAusbeute 81,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To the solution of 5-bromo-6-methoxy-7-methylquinoline (6.5 g, 25.8 mmol) in DCM (150 mL) was added BBr3 slowly (77.3 mL, 1.0 M in DCM, 77.3 mmol). The mixture was stirred for 3 hours and cooled to 0° C. Methanol (40 mL) was added slowly and the mixture was stirred for 20 minutes. The solvents were removed under reduced pressure. The solid was dissolved in methanol (100 mL) and was treated with 1.0 N sodium hydroxide solution (50 mL) (pH ˜12). The mixture was stirred for 12 hours and acetic acid was added to adjust pH to between 4-5. The mixture was filtered and washed with water. The gray solid was dried under reduced pressure to give 5-bromo-7-methylquinolin-6-ol (5.0 g). LCMS-ESI+ (m/z): 238.2, 240.1 (M+H)+, 236.1, 238.0 (M−H).

Aufarbeitung

  1. stirringthe mixture was stirred for 20 minutes
  2. customThe solvents were removed under reduced pressure
  3. dissolutionThe solid was dissolved in methanol (100 mL)
  4. additionwas treated with 1.0 N sodium hydroxide solution (50 mL) (pH ˜12)
  5. stirringThe mixture was stirred for 12 hours
  6. additionacetic acid was added
  7. filtrationThe mixture was filtered
  8. washwashed with water
  9. customThe gray solid was dried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-7bac8e3398b043f1b0b7d5374a40c5b2
Quelldatensatz
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09296758B2

Notizen zur Reaktion

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