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Succinic anhydride → 4-(4-Bromo-2-methylphenyl)-4-oxobutanoic acid

HRID 735637
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반응식

HRID 735637 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5](I)=[C:4]([CH3:9])[CH:3]=1.C([Mg]Br)(C)C.[C:15]1(=[O:21])[O:20][C:18](=[O:19])[CH2:17][CH2:16]1>C1COCC1>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:15](=[O:21])[CH2:16][CH2:17][C:18]([OH:20])=[O:19])=[C:4]([CH3:9])[CH:3]=1
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참가 물질

5

반응물 3

HCID 7922Succinic anhydrideHCID 27246015-Bromo-2-iodotolueneHCID 178418365HCID 178418365, 화합물

생성물 1

HCID 247270004-(4-Bromo-2-methylphenyl)-4-oxobutanoic acid수율 31%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 4-bromo-1-iodo-2-methylbenzene (148 mg, 0.5 mmol) in THF (10 mL) at −25° C. was added isopropylmagnesium bromide (0.5 mL, 0.5 mmol) and stirred 3 h. Succinic anhydride (55 mg, 0.55 mmol) was added and the reaction was stirred 18 h. The mixture was quenched with water (10 mL) and washed with 1N NaOH (10 mL), 1N HCl (10 mL), brine (10 mL) and dried (MgSO4). The organic layer was concentrated in vacuo and the residue purified by flash chromatography (0-100% EtOAc/Hexane) to afford 55A (42 mg, 31%) as a crystalline solid. 1H NMR (400 MHz, CDCl3) δ ppm 0.98 (t, 3 H) 2.42 (q, 2 H) 2.73 (t, 2 H) 4.10 (t, 2 H) 6.82 (d, 1 H) 7.02 (d, 1 H) 7.09 (t, 2 H) 7.15 (t, 1 H) 7.36 (d, 1 H) 7.58-7.63 (m, 1 H).

후처리

  1. stirringthe reaction was stirred 18 h
  2. customThe mixture was quenched with water (10 mL)
  3. washwashed with 1N NaOH (10 mL), 1N HCl (10 mL), brine (10 mL)
  4. dry with materialdried (MgSO4)
  5. concentrationThe organic layer was concentrated in vacuo
  6. customthe residue purified by flash chromatography (0-100% EtOAc/Hexane)

출처 및 근거

ORD 기록
ord-7a8fab20a3e84cb185831c372aee819c
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07592331B2

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