Triethylamine → 2-Fluoro-4-vinylbenzonitrile

HRID 1502069노트

반응식

HRID 1502069 반응식
CS(O[CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([C:14]#[N:15])=[C:10]([F:16])[CH:9]=1)(=O)=O.C(N(CC)CC)C.C1CCN2C(=NCCC2)CC1>C(Cl)Cl>[CH:7]([C:8]1[CH:13]=[CH:12][C:11]([C:14]#[N:15])=[C:10]([F:16])[CH:9]=1)=[CH2:6]

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 866473092-(4-Cyano-3-fluorophenyl)ethyl methanesulfonate

생성물 1

HCID 219046072-Fluoro-4-vinylbenzonitrile

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

A solution of 2-(4-cyano-3-fluorophenyl)ethyl methanesulfonate (35.0 g, 144 mmol) and triethylamine (50 mL) in DCM (200 mL) was added DBU (50 mL) dropwise to at 0° C. After stirring at room temperature overnight, the solution was diluted with DCM, washed with 1 N HCl and brine, and dried over anhydrous sodium sulphate and concentrated. The residue was purified by column chromatography to give title compound.

후처리

  1. washwashed with 1 N HCl and brine
  2. dry with materialdried over anhydrous sodium sulphate
  3. concentrationconcentrated
  4. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-5114ddd5f6e34238904340d310b7f752
출처 데이터셋
uspto-grants-2015_12
특허 번호
US09206199B2

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