N-bromobutanimide → HCID 118143116、化合物

HRID 523956

反応式

HRID 523956 の反応式
[NH2:1][C:2]1[C:10]2[O:9][C:8]([F:12])([F:11])[O:7][C:6]=2[CH:5]=[CH:4][CH:3]=1.[Br:13]N1C(=O)CCC1=O>ClCCl>[Br:13][C:3]1[CH:4]=[CH:5][C:6]2[O:7][C:8]([F:12])([F:11])[O:9][C:10]=2[C:2]=1[NH2:1]

参加物

4

反応条件

温度
0 °C

実験手順

To a stirred solution of 4-amino-2,2-diflouro-1,3-benzodioxole (2.5 g, 14.4 mmol) in dichloromethane at 0° C. was added N-bromosuccinimide (2.7 g, 15.2 mmol) portion wise. The solution was stirred at 0° C. for 30 min, then at room temperature for 1 h. The reaction mixture was quenched with 1M sodium thiosulfate solution and diluted with deionized water, extracted with dichloromethane (2×50 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, 0-20% ethyl acetate in hexanes) to recover starting material 1 g and afford 5-bromo-4-amino-2,2-diflouro-1,3-benzodioxole as colorless oil (2.33 g, 9.25 mmol, 64%). MS: (ES) m/z calculated for C7H4BrF2NO [M+H]+252.0. found 252.

後処理

  1. waitat room temperature for 1 h
  2. customThe reaction mixture was quenched with 1M sodium thiosulfate solution
  3. additiondiluted with deionized water
  4. extractionextracted with dichloromethane (2×50 mL)
  5. dry with materialThe combined organic layers were dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude product was purified by flash chromatography (SiO2, 0-20% ethyl acetate in hexanes)
  9. customto recover

出典と根拠

ORDレコード
ord-ca80740c073c413ca1f23ddfff5a55c5
出典データセット
uspto-grants-2016_05
特許番号
US09340509B2

関連ノート

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