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Hydrochloric Acid → 3,5-Difluorophenyl boric acid

HRID 566160
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HRID 566160 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

HCID 222378233,5-Difluorophenyl boric acid수율 70%

시약·촉매·용매 2

HCID 8028Tetrahydrofuran용매2회
HCID 8058
Hexane
용매

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-110493de4abc4b5885b16cf9c800fca6
출처 데이터셋
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06174458B1

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