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N-bromobutanimide → HCID 71237985, 화합물

HRID 340066
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HRID 340066 반응식
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([F:9])=[C:5]([O:10][CH3:11])[CH:4]=1)[CH3:2].C1C(=O)N([Br:19])C(=O)C1>CC#N>[Br:19][C:8]1[CH:7]=[C:6]([F:9])[C:5]([O:10][CH3:11])=[CH:4][C:3]=1[CH2:1][CH3:2]
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참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 597891854-Ethyl-1-fluoro-2-methoxybenzene

생성물 1

HCID 71237985HCID 71237985, 화합물수율 97.6%

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

To a solution of 4-ethyl-1-fluoro-2-methoxy-benzene (WO 2010/090537, 12.2 g, 79.1 mmol) in MeCN (150 mL) was added a solution of NBS (14.4 g, 80.7 mmol) in MeCN (50 mL). The resulting solution was stirred at room temperature for 18 hours. The solvent was removed in vacuo and the residue was diluted with diethyl ether (150 mL). Precipitated solid was removed by filtration and the filtrate was washed with sodium sulfite aqueous solution (100 mL) and brine (100 mL), dried over MgSO4 and concentrated in vacuo to give the title compound as a yellow oil (18 g) in a 97% yield.

후처리

  1. customThe solvent was removed in vacuo
  2. additionthe residue was diluted with diethyl ether (150 mL)
  3. customPrecipitated solid
  4. customwas removed by filtration
  5. washthe filtrate was washed with sodium sulfite aqueous solution (100 mL) and brine (100 mL)
  6. dry with materialdried over MgSO4
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-ead066270813402393b301a8d5deb296
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08895544B2

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