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2-Propen-1-yl 1,1,1-trifluoromethanesulfonate → 5,6-Dimethoxy-2-methyl-3-(2-propen-1-yl)benzotellurazolium Trifluoromethanesulfonate

HRID 543085
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HRID 543085 반응식
[F:1][C:2]([F:11])([F:10])[S:3]([O:6][CH2:7][CH:8]=[CH2:9])(=[O:5])=[O:4].[CH3:12][O:13][C:14]1[C:15]([O:24][CH3:25])=[CH:16][C:17]2[Te:21][C:20]([CH3:22])=[N:19][C:18]=2[CH:23]=1>C(Cl)(Cl)(Cl)Cl.ClCCl>[F:1][C:2]([F:11])([F:10])[S:3]([O-:6])(=[O:5])=[O:4].[CH3:12][O:13][C:14]1[C:15]([O:24][CH3:25])=[CH:16][C:17]2[Te:21][C:20]([CH3:22])=[N+:19]([CH2:9][CH:8]=[CH2:7])[C:18]=2[CH:23]=1
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참가 물질

5

반응물 2

HCID 109322232-Propen-1-yl 1,1,1-trifluoromethanesulfonateHCID 139312085,6-Dimethoxy-2-methylbenzotellurazole

생성물 1

HCID 143241435,6-Dimethoxy-2-methyl-3-(2-propen-1-yl)benzotellurazolium Trifluoromethanesulfonate

시약·촉매·용매 2

HCID 5943Carbon Tetrachloride용매HCID 6344Dichloromethane용매

실험 절차

A dried solution of 2-propen-1-yl tri-fluoromethanesulfonate (0.002 mole) in carbon tetrachloride was added dropwise to a solution of 5,6-dimethoxy-2-methylbenzotellurazole (Example 19) (0.50 g, 0.0016 mole) in dichloromethane (25 ml) under a nitrogen atmosphere at room temperature. After the addition was complete, stirring was continued for 7 hours. The solid was isolated by filtration, washed with diethyl ether, and dried at room temperature under vacuum. Yield 0.38 g. A mass spectrogram of the compound was in agreement with that expected for the structural formula.

후처리

  1. additionAfter the addition
  2. customThe solid was isolated by filtration
  3. washwashed with diethyl ether
  4. customdried at room temperature under vacuum

출처 및 근거

ORD 기록
ord-c77d63ecb57d46b79b5b9d297ff5355c
출처 데이터셋
uspto-grants-1987_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04661438

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