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Hydrochloric Acid → 3,5-Difluorophenyl boric acid

HRID 566160
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 566160
Br[C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[C:4]([F:9])[CH:3]=1.C([Li])CCC.[B:15]([O:24]C(C)C)([O:20]C(C)C)[O:16]C(C)C.Cl>CCCCCC.C1COCC1>[F:9][C:4]1[CH:3]=[C:2]([O:16][B:15]([OH:24])[OH:20])[CH:7]=[C:6]([F:8])[CH:5]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 1363131-Bromo-3,5-difluorobenzeneHCID 178418339Butyllithium

Produkt 1

HCID 222378233,5-Difluorophenyl boric acidAusbeute 70 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 8028
Tetrahydrofuran
Lösungsmittel
2×
HCID 8058HexaneLösungsmittel

Versuchsvorschrift

To a mixture of 1-bromo-3,5-difluorobenzene (743 mmol) and 500 ml of THF was added dropwise 500 ml of a solution of n-butyl lithium (corresponding to 780 mmol) in hexane at −78° C. in 1.6 hours, and stirred at the same temperature for 1.5 hours. To this solution was wadded dropwise 200 ml of a solution of triisopropyl borate (1,486 mmol) in THF, the solution was gradually warmed up to room temperature, and then the solution was stirred overnight. After 750 ml of 7.3% hydrochloric acid was added and stirred for 30 min, the reaction solution was extracted twice with diethyl ether, washed thrice with water, and then dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was recrystallized from about 1,000 ml of toluene to give a white solid of 3,5-difluorophenyl boric acid (520 mmol).

Aufarbeitung

  1. stirringthe solution was stirred overnight
  2. stirringstirred for 30 min
  3. extractionthe reaction solution was extracted twice with diethyl ether
  4. washwashed thrice with water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. distillationThe solvent was distilled off
  7. customthe residue was recrystallized from about 1,000 ml of toluene

Quellen und Nachweise

ORD-Eintrag
ord-110493de4abc4b5885b16cf9c800fca6
Quelldatensatz
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06174458B1

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