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

HRID 588805
ノート
印刷プレビュー

反応式

HRID 588805 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 62652Cuprous chloride触媒HCID 887Methanol溶媒

実験手順

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]+.

後処理

  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)

出典と根拠

ORDレコード
ord-84a01c8671a245809dca9c8cb91b8a6d
出典データセット
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09227978B2

反応ノート

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