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5-Bromo-2-(4-methoxybenzyl)-3,3-dimethylisoindolin-1-one → 5-Bromo-3,3-dimethyl-isoindolin-1-one

HRID 1784002
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HRID 1784002 반응식
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[N:6](CC1C=CC(OC)=CC=1)[C:5]2([CH3:22])[CH3:21]>C(#N)C.O.C(OCC)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[NH:6][C:5]2([CH3:22])[CH3:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 575899515-Bromo-2-(4-methoxybenzyl)-3,3-dimethylisoindolin-1-one

생성물 1

HCID 575899965-Bromo-3,3-dimethyl-isoindolin-1-one수율 86%

시약·촉매·용매 3

HCID 962Water용매HCID 6342Acetonitrile용매HCID 8857Ethyl Acetate용매

실험 절차

A solution of 5-bromo-2-(4-methoxybenzyl)-3,3-dimethyl-2,3-dihydroisoindol-1-one (640 mg, 1.78 mmol) and ceric ammonium nitrate (2.91 g, 5.33 mmol) in acetonitrile (11 mL) and water (5 mL) is stirred at 0° C. for 45 min. The solution is diluted with ethyl acetate (100 mL) and washed with brine (40 mL). The organic solvents are dried over MgSO4 and evaporated under reduced pressure. The residue is purified by silica chromatography, eluting with 10% to 50% ethyl acetate in petroleum ether to afford the title compound (367 mg, 1.53 mmol).

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후처리

  1. washwashed with brine (40 mL)
  2. dry with materialThe organic solvents are dried over MgSO4
  3. customevaporated under reduced pressure
  4. customThe residue is purified by silica chromatography
  5. washeluting with 10% to 50% ethyl acetate in petroleum ether

출처 및 근거

ORD 기록
ord-3eae8be13edb415e92dc28b5f0766434
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07501411B2

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