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Boron tribromide → 2,3-Difluoro-4-methyl-5-nitro-phenol

HRID 2065745
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2065745
COC(=O)[O:4][C:5]1[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[C:8]([CH3:14])=[C:7]([F:15])[C:6]=1[F:16].B(Br)(Br)Br>ClCCl>[F:16][C:6]1[C:7]([F:15])=[C:8]([CH3:14])[C:9]([N+:11]([O-:13])=[O:12])=[CH:10][C:5]=1[OH:4]
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Komponenten

4

Edukt 2

HCID 25134Boron tribromideHCID 59377938Carbonic acid 2,3-difluoro-4-methyl-5-nitro-phenyl ester methyl ester

Produkt 1

HCID 593779072,3-Difluoro-4-methyl-5-nitro-phenolAusbeute 58 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

A solution of carbonic acid 2,3-difluoro-4-methyl-5-nitro-phenyl ester methyl ester (2.3 g, 9.3 mmol) in dichloromethane (30 ml) was cooled to 0° C. in an ice bath, and 1.0M boron tribromide in dichloromethane (9.3 ml, 9.3 mmol) was added. The ice-bath was removed and the mixture was stirred at room temperature for 18 hours. Water was added and the mixture was extracted with EtOAc. The combined extracts were washed with water and brine, dried over MgSO4, filtered and concentrated to dryness under reduced pressure. Purification of the crude product by flash chromatography (hexanes:EtOAc 9:1) gave 1.02 g (58%) of 2,3-difluoro-4-methyl-5-nitro-phenol as a white solid.

Aufarbeitung

  1. customThe ice-bath was removed
  2. additionWater was added
  3. extractionthe mixture was extracted with EtOAc
  4. washThe combined extracts were washed with water and brine
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated to dryness under reduced pressure
  8. customPurification of the crude product by flash chromatography (hexanes:EtOAc 9:1)

Quellen und Nachweise

ORD-Eintrag
ord-1ff7a241f398436b863a577cfe1db708
Quelldatensatz
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08288552B2

Notizen zur Reaktion

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