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Boron tribromide → 4-Cyclopropyl-3-fluoro-2-hydroxybenzaldehyde

HRID 2272519
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2272519
B(Br)(Br)Br.[CH:5]1([C:8]2[CH:15]=[CH:14][C:11]([CH:12]=[O:13])=[C:10]([O:16]C)[C:9]=2[F:18])[CH2:7][CH2:6]1.C(=O)(O)[O-].[Na+]>ClCCl>[CH:5]1([C:8]2[CH:15]=[CH:14][C:11]([CH:12]=[O:13])=[C:10]([OH:16])[C:9]=2[F:18])[CH2:6][CH2:7]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 25134Boron tribromideHCID 516892Sodium BicarbonateHCID 904232524-Cyclopropyl-3-fluoro-2-methoxybenzaldehyde

Produkt 1

HCID 904235724-Cyclopropyl-3-fluoro-2-hydroxybenzaldehydeAusbeute 90,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

Boron tribromide (1 M dichloromethane solution, 18.5 mL) was added at −78 C to a dichloromethane (70 mL) solution of 4-cyclopropyl-3-fluoro-2-methoxybenzaldehyde (1.79 g), and the mixture was stirred at the same temperature as above for 2 hours in a nitrogen atmosphere and then stirred at 0 C for 1 hour. A saturated aqueous solution of sodium bicarbonate was added to the reaction mixture at 0 C, and dichloromethane was distilled off under reduced pressure. The obtained residue was subjected to extraction with ethyl acetate. The obtained organic layer was washed with water and saturated saline in this order and dried over anhydrous magnesium sulfate, and then, the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to obtain the title compound (1.50 g).

Aufarbeitung

  1. stirringstirred at 0 C for 1 hour
  2. distillationwas distilled off under reduced pressure
  3. extractionThe obtained residue was subjected to extraction with ethyl acetate
  4. washThe obtained organic layer was washed with water and saturated saline in this order
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled off under reduced pressure
  7. customThe obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate)

Quellen und Nachweise

ORD-Eintrag
ord-1d4006afa2de4a21a1aa68dc376f7644
Quelldatensatz
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09120777B2

Notizen zur Reaktion

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