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Trifluoromethanesulfonic acid → 1-Chloro-2,5-difluoro-4-iodobenzene

HRID 1480580
ノート
印刷プレビュー

反応式

HRID 1480580 の反応式
FC(F)(F)S(O)(=O)=O.[Cl:9][C:10]1[CH:15]=[C:14]([F:16])[CH:13]=[CH:12][C:11]=1[F:17].[I:18]N1C(=O)CCC1=O>>[Cl:9][C:10]1[CH:15]=[C:14]([F:16])[C:13]([I:18])=[CH:12][C:11]=1[F:17]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 62406Trifluoromethanesulfonic acidHCID 120273N-IodosuccinimideHCID 1375611-Chloro-2,5-difluorobenzene

生成物 1

HCID 510000881-Chloro-2,5-difluoro-4-iodobenzene収率 77.5%

反応条件

温度
0 °C

実験手順

Trifluoromethanesulfonic acid (9.9 mL, 110 mmol) was added to 2-chloro-1,4-difluorobenzene (2.2 g, 15 mmol) at room temperature and then cooled to 0° C. N-Iodosuccinimide (3.16 g, 14.1 mmol) was then added in multiple portions. After 10 minutes, the reaction mixture was allowed to warm to room temperature and stirred for 2 hours. The reaction mixture was poured over ice-water and extracted with hexane. The organic layer was washed with saturated Na2SO4, dried and concentrated. The crude product was purified by silica gel chromatography (100% hexanes) to give 1-chloro-2,5-difluoro-4-iodobenzene (3.0 g, 74%). 1H NMR (400 MHz, CDCl3) δ 7.52 (dd, J=5.4, 7.8, 1H), 7.17-7.08 (m, 1H).

後処理

  1. temperatureto warm to room temperature
  2. extractionextracted with hexane
  3. washThe organic layer was washed with saturated Na2SO4
  4. customdried
  5. concentrationconcentrated
  6. customThe crude product was purified by silica gel chromatography (100% hexanes)

出典と根拠

ORDレコード
ord-c6bb46bd04d54b9da2a0f0fbc0b9de59
出典データセット
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09409886B2

反応ノート

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