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2,4-Dimethoxybenzaldehyde → 5-{[(2,4-Dimethoxyphenyl)methyl]amino}-2-benzofuran-1(3H)-one

HRID 1829025
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HRID 1829025 반응식
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:7](=[O:8])[O:6][CH2:5]2.[CH3:12][O:13][C:14]1[CH:21]=[C:20]([O:22][CH3:23])[CH:19]=[CH:18][C:15]=1[CH:16]=O.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>CC(O)=O.CN(C=O)C.CCOC(C)=O>[CH3:12][O:13][C:14]1[CH:21]=[C:20]([O:22][CH3:23])[CH:19]=[CH:18][C:15]=1[CH2:16][NH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:7](=[O:8])[O:6][CH2:5]2
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참가 물질

6

반응물 3

HCID 691752,4-DimethoxybenzaldehydeHCID 7206695-AminophthalideHCID 5049666Sodium triacetoxyborohydride

생성물 1

HCID 220615235-{[(2,4-Dimethoxyphenyl)methyl]amino}-2-benzofuran-1(3H)-one수율 82%

시약·촉매·용매 2

HCID 8857Ethyl Acetate용매
HCID 21926011
acetic acid N,N-dimethylformamide
용매

실험 절차

To a stirred solution of 5-aminophthalide (11.7 g, 78 mmol) and 2,4-dimethoxybenzaldehyde (15.5 g, 93.6 mmol) in 1% AcOH/DMF (60 ml), was added sodium triacetoxyborohydride (50.0 g, 236 mmol). The mixture was stirred at room temperature for 16 hours, diluted with EtOAc (400 ml), washed with saturated NaHCO3 solution (3×400 ml) and water (400 ml), dried over anhydrous Na2SO4, and evaporated to provide a crude product. Trituration of the crude product with MEOH gave 5-(2,4-dimethoxy-benzylamino)-3H-isobenzofuran-1-one as an off-white powder (19.0 g, 82%).

후처리

  1. washwashed with saturated NaHCO3 solution (3×400 ml) and water (400 ml)
  2. dry with materialdried over anhydrous Na2SO4
  3. customevaporated
  4. customto provide a crude product

출처 및 근거

ORD 기록
ord-27fc80294c8f45dcb84fe3afefd21b46
출처 데이터셋
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07060844B2

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