Hydrochloric Acid → 3,3'-Difluoro-4-propoxybiphenyl
반응식
[F:1][C:2]1[CH:3]=[C:4](Br)[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][CH2:10][CH3:11].OB(O)[C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=1.FC1C=C(Br)C=CC=1.[Mg].COB(OC)OC.Cl.C([O-])([O-])=O.[K+].[K+]>[Pd].CCCCCCC.C1(C)C=CC=CC=1.C1(C)C=CC=CC=1.C(O)C.O>[F:1][C:2]1[CH:3]=[C:4]([C:15]2[CH:20]=[CH:19][CH:18]=[C:17]([F:21])[CH:16]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH2:9][CH2:10][CH3:11]참가 물질
반응물 7
생성물 1
시약·촉매·용매 3
실험 절차
A mixture of 22.0 g (94.4 mmol) of 3-fluoro-4-propoxybromobenzene, 22.5 g (141.6 mmol) of dihydroxy(3-fluorophenyl)borane (prepared by reacting a Grignard reagent, which was prepared from 3-fluorobromobenzene and magnesium, with trimethoxyborane, and then hydrolysing with hydrochloric acid), 26.1 g (188.8 mmol) of K2CO3, 2.0 g of 5%Pd—C, and 150 ml of mixed solvent of toluene/ethanol/water (1/1/1) was heated to reflux for 27 hours. Subsequently, the Pd—C was removed by filtration, the mixture was extracted with 150 ml of toluene, the organic layer thus obtained was washed with water thrice, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under a reduced pressure, and the residue thus obtained was subjected to silica gel column chromatography (eluent: heptane/toluene=1/1) to obtain 20.1 g of a crude 3,3′-difluoro-4-propoxybiphenyl. (Yield: 86.1%)
후처리
- customprepared
- temperaturewas heated
- temperatureto reflux for 27 hours
- customSubsequently, the Pd—C was removed by filtration
- extractionthe mixture was extracted with 150 ml of toluene
- customthe organic layer thus obtained
- washwas washed with water thrice
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe solvent was distilled off under a reduced pressure
- customthe residue thus obtained
출처 및 근거
- ORD 기록
- ord-8261f870b20b4cb68712e89c71310e11
- 출처 데이터셋
- uspto-grants-2001_03
- 특허 번호
- US06197217B1
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