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Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1) → 4,6-Dichloro-1,2-dimethylquinolinium tetrafluoroborate

HRID 2118596
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반응식

HRID 2118596 반응식
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[N:5]=[C:4]([CH3:13])[CH:3]=1.[F:14][B-:15]([F:18])([F:17])[F:16].[CH3:19][O+](C)C>C(#N)C>[F:14][B-:15]([F:18])([F:17])[F:16].[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Cl:12])[CH:10]=2)[N+:5]([CH3:19])=[C:4]([CH3:13])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2735153Oxonium, trimethyl-, tetrafluoroborate(1-) (1:1)HCID 123225774,6-Dichloro-2-methylquinoline

생성물 1

HCID 200290004,6-Dichloro-1,2-dimethylquinolinium tetrafluoroborate수율 78.8%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

The starting material may be prepared as follows. Powdered 4,6-dichloro-2-methylquinoline (254 mg.) was added to a stirred solution of trimethyloxonium tetrafluoroborate (177 mg.) in acetonitrile (1 ml.), and stirring was continued overnight. The solvent was evaporated and the residue was triturated with ether to give 4,6-dichloro-1,2-dimethylquinolinium tetrafluoroborate (296 mg.). N.m.r. in solvent A: 3.07(s, 3H); 4.44(s, 3H); 7.9-8.8(complex, 4H).

후처리

  1. customThe starting material may be prepared
  2. customThe solvent was evaporated
  3. customthe residue was triturated with ether

출처 및 근거

ORD 기록
ord-5ad3f30b3de1403aa8cd019171bb9eb5
출처 데이터셋
uspto-grants-1987_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04678781

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