4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl

4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl 구조식 이미지
카스 번호:
916156-32-6
상품명:
4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl
동의어(영문):
Penta-2,6,2 '- trifluoromethyl-3,4,5-trifluorobenzene;4-[Difluoro-(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1'4',1''-terphenyl;4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl;1,1':4',1''-Terphenyl, 4-[difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-
CBNumber:
CB12717325
분자식:
C30H22F8O
포뮬러 무게:
550.48
MOL 파일:
916156-32-6.mol

4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl 속성

안전

기존화학 물질 2013-3-5676

4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl C화학적 특성, 용도, 생산

제조 방법

The preparation of 4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl is as follows:10.0 g (29.0 mmol) of 5-[4-chloro-2,6-difluorophenyl)difluoromethoxy]-1,2,3-trifluorobenzene and 8.47 g (29.6 mmol, 1.02 equivalent amount) of 4'-pentyl-3-fluoro-4-biphenylboronic acid were placed in a 300-ml SUS autoclave, after which 467 mg (0.05 equivalent amount) of TBAB, 16.6 mg (0.0012 equivalent amount) of 2-dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl (purchased from Johnson Matthey Japan Inc.), and 49.4 mg (0.0004 equivalent amount) of 5% palladium carbon were placed in the autoclave. The autoclave was subsequently sealed, and the atmosphere therein was replaced with nitrogen. Thereafter, 30 ml of deaerated water and 10 ml of deaerated DMAc was added thereto, and 4.5 g (1.5 equivalent amount) of triethylamine was further added thereto, followed by stirring at the reaction liquid temperature of 99°C for 4 hours. The mixture was stirred at room temperature for 20 minutes, and 50 ml of toluene and 30 ml of water were added to the reaction mixture, followed by additional stirring for 15 minutes. The reaction yield was 97.7% (quantified by 19F NMR). The organic layer was subjected to suction filtration (using Celite), the filtrate was concentrated, and then the residue was purified using column chromatography. The crude substance thus obtained was recrystallized with a mixed solvent of denatured ethanol and heptane, thereby obtaining 4-[difluoro-(3,4,5-trifluoro-phenoxy)-methyl]-2',3,5-trifluoro-4"-pentyl-[1,1';4',1"]terphenyl in the form of a white solid. Amount obtained: 14.8 g (isolation yield 93.0%, purity 99.9%). 

916156-32-6.png

4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl 준비 용품 및 원자재

원자재

준비 용품


4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl 공급 업체

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4-[Difluoro(3,4,5-trifluorophenoxy)methyl]-2',3,5-trifluoro-4''-pentyl-1,1':4',1''-terphenyl 관련 검색:

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