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Borohydride → (2-Amino-5-bromo-3-fluorophenyl)methanol

HRID 56469
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 56469
[NH2:1][C:2]1[C:10]([F:11])=[CH:9][C:8]([Br:12])=[CH:7][C:3]=1[C:4](O)=[O:5].[BH4-]>C1COCC1>[NH2:1][C:2]1[C:10]([F:11])=[CH:9][C:8]([Br:12])=[CH:7][C:3]=1[CH2:4][OH:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 28123BorohydrideHCID 404245972-Amino-5-bromo-3-fluorobenzoic acid

Produkt 1

HCID 54312525(2-Amino-5-bromo-3-fluorophenyl)methanolAusbeute 95 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of 2-amino-5-bromo-3-fluorobenzoic acid (14.5 g, 62.2 mmol) in THF (150 mL) at 0° C. was added borohydride in THF (1 M, 310 mL), and the reaction mixture was stirred at room temperature overnight. The reaction was quenched with methanol (150 mL), concentrated in vacuum, diluted with aqueous sodium bicarbonate (400 mL) and extracted with ethyl acetate (200 mL*3). The organic layers were separated, combined, washed with water (200 mL) and brine (200 mL), dried over sodium sulfate, filtered and concentrated to afford the title compound (13.0 g, crude), which was directly used in the next step without the further purification. MS (ES+) C7H7BrFNO requires: 219, 221, found: 220, 222 [M+H]+.

Aufarbeitung

  1. customThe reaction was quenched with methanol (150 mL)
  2. concentrationconcentrated in vacuum
  3. additiondiluted with aqueous sodium bicarbonate (400 mL)
  4. extractionextracted with ethyl acetate (200 mL*3)
  5. customThe organic layers were separated
  6. washwashed with water (200 mL) and brine (200 mL)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-cbaeea48176b456eaf135dbfa41aeec5
Quelldatensatz
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09434700B2

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