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Sodium borohydride → 2',6-Dichloro-4-ethyl-[1,1'-biphenyl]-3-amine

HRID 588805
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HRID 588805 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:13]([Cl:14])=[CH:12][C:11]([CH:15]=[CH2:16])=[C:10]([NH2:17])[CH:9]=1.[BH4-].[Na+]>CO.Cl[Cu]>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[C:13]([Cl:14])=[CH:12][C:11]([CH2:15][CH3:16])=[C:10]([NH2:17])[CH:9]=1
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 904603862',6-Dichloro-4-vinyl-[1,1'-biphenyl]-3-amine

생성물 1

HCID 904625672',6-Dichloro-4-ethyl-[1,1'-biphenyl]-3-amine수율 59.4%

시약·촉매·용매 2

HCID 62652Cuprous chloride촉매HCID 887Methanol용매

실험 절차

A mixture of 2′,6-dichloro-4-vinyl-[1,1′-biphenyl]-3-amine (500 mg, 1.9 mmol), CuCl (225 mg, 2.28 mmol) in MeOH (10 mL) at 0° C., NaBH4 (722 mg, 19 mmol) was added in portions and the resulting mixture was stirred at room temperature for 20 min. The reaction was quenched with water and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (petroleum ether/ethyl acetate=30:1) to afford the desired product (300 mg, 59.4% yield). ESI-MS m/z: 266.0[M+H]+.

후처리

  1. customThe reaction was quenched with water
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by flash column chromatography on silica gel (petroleum ether/ethyl acetate=30:1)

출처 및 근거

ORD 기록
ord-84a01c8671a245809dca9c8cb91b8a6d
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227978B2

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