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Ethanol → (2-Methoxy-[1,1'-biphenyl]-4-yl)methanamine

HRID 1713281
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반응식

HRID 1713281 반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:9][N:10]2C(=O)C3=CC=CC=C3C2=O)[CH:6]=[CH:5][C:4]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.C(O)C>C(Cl)(Cl)Cl>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([CH2:9][NH2:10])[CH:6]=[CH:5][C:4]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1
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참가 물질

4

반응물 2

HCID 702EthanolHCID 67453881HCID 67453881, 화합물

생성물 1

HCID 23143909(2-Methoxy-[1,1'-biphenyl]-4-yl)methanamine수율 100.7%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

To a solution of N-(2-methoxybiphenyl-4-ylmethyl)-phthalimide (0.414 g) in chloroform (5.0 mL) was added dropwise a mixture of hydrazinemonohydrate (0.241 g) and ethanol (1.0 mL), and the resulting mixture was stirred at room temperature for 31 hours. The insoluble material was filtered out, and the filtrate was partitioned between dichloromethane (40 mL) and water (15 mL). The organic layer was washed with brine (10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the title compound (0.259 g).

후처리

  1. filtrationThe insoluble material was filtered out
  2. customthe filtrate was partitioned between dichloromethane (40 mL) and water (15 mL)
  3. washThe organic layer was washed with brine (10 mL)
  4. dry with materialdried over anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-82a565650c1c4da389c3d0116156fb3f
출처 데이터셋
uspto-grants-2010_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07795236B2

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