ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Methyl 5-bromo-2-iodobenzoate → Methyl 5-bromo-2-ethylbenzoate

HRID 1749376
ノート
印刷プレビュー

反応式

HRID 1749376 の反応式
C([Zn][CH2:4][CH3:5])C.[Br:6][C:7]1[CH:8]=[CH:9][C:10](I)=[C:11]([CH:16]=1)[C:12]([O:14][CH3:15])=[O:13]>Cl>[Br:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:4][CH3:5])=[C:11]([CH:16]=1)[C:12]([O:14][CH3:15])=[O:13]
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 2

HCID 11078356Methyl 5-bromo-2-iodobenzoateHCID 178418750HCID 178418750、化合物

生成物 1

HCID 44226584Methyl 5-bromo-2-ethylbenzoate収率 176.1%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

反応条件

温度
62.5 °C

実験手順

Add diethyl zinc (3050 mL, 3.05 mol, 1 M hexane) over 3 hours to a 5° C. solution of methyl 5-bromo-2-iodobenzoate (1876 g, 5.50 mol) and (1,1′-bis(diphenylphosphino)ferrocene)palladium(II) chloride (40 g, 0.05 mol). Heat the mixture to 60-65° C. over 2 hours and stir for an additional 2 hours, then cool to 10-15° C. and pour into ice cold aqueous 1 M HCl (10 L). Separate the phases, extract the aqueous layer with methyl-tert-butyl ether (2×10 L), combine the organic phases, wash with saturated aqueous sodium chloride, dry over sodium sulfate, filter, and evaporate under reduced pressure. Dissolve in ethyl acetate (400 mL) and add petroleum ether (8 L), then let stand at 15-20° C. for 16 hours and filter through a pad of silica gel, wash with ethyl acetate/petroleum ether (1:20, 8 L) and evaporate the filtrate under reduced pressure to provide the title compound as a pale yellow oil (1306 g, 96%). ES/MS m/e: (79Br/81Br) 243/245 (M+H).

後処理

  1. temperaturecool to 10-15° C.
  2. customSeparate the phases
  3. extractionextract the aqueous layer with methyl-tert-butyl ether (2×10 L)
  4. washwash with saturated aqueous sodium chloride
  5. dry with materialdry over sodium sulfate
  6. filtrationfilter
  7. customevaporate under reduced pressure
  8. dissolutionDissolve in ethyl acetate (400 mL)
  9. additionadd petroleum ether (8 L)
  10. waitlet stand at 15-20° C. for 16 hours
  11. filtrationfilter through a pad of silica gel
  12. washwash with ethyl acetate/petroleum ether (1:20, 8 L)
  13. customevaporate the filtrate under reduced pressure

出典と根拠

ORDレコード
ord-ed2ad25913ae461d8980f86367ddf22f
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09156824B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート