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Pyridine → HCID 57787275, 화합물

HRID 2426771
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HRID 2426771 반응식
[F:1][C:2]([F:15])([F:14])[S:3]([O:6]S(C(F)(F)F)(=O)=O)(=[O:5])=[O:4].O[C:17]1[CH:22]=[CH:21][C:20]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([CH2:29][O:30][C:31]3[CH:38]=[CH:37][C:34]([CH:35]=[O:36])=[CH:33][CH:32]=3)[C:24]=2[CH3:39])=[C:19]([CH3:40])[CH:18]=1.N1C=CC=CC=1>ClCCl>[F:1][C:2]([F:15])([F:14])[S:3]([O:6][C:17]1[CH:22]=[CH:21][C:20]([C:23]2[CH:28]=[CH:27][CH:26]=[C:25]([CH2:29][O:30][C:31]3[CH:32]=[CH:33][C:34]([CH:35]=[O:36])=[CH:37][CH:38]=3)[C:24]=2[CH3:39])=[C:19]([CH3:40])[CH:18]=1)(=[O:5])=[O:4]
참가 물질반응 조건실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1049PyridineHCID 67749Trifluoromethanesulfonic anhydrideHCID 57787806HCID 57787806, 화합물

생성물 1

HCID 57787275HCID 57787275, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

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온도
0 °C

실험 절차

Trifluoromethanesulfonic anhydride was dropwise added under ice-cooling to a mixture of 4-[(4′-hydroxy-2,2′-dimethylbiphenyl-3-yl)methoxy]benzaldehyde, pyridine and dichloromethane; followed by stirring at 0° C. for 1 hour to obtain 3′-[(4-formylphenoxy)methyl]-2,2′-dimethylbiphenyl-4-yl trifluoromethanesulfonate.

출처 및 근거

ORD 기록
ord-c40c21177c744f4d8f23db83f7f87873
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968552B2

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