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

Potassium Carbonate → 3-Bromo-2-methyl-1-benzofuran

HRID 2181682
ノート
印刷プレビュー

反応式

HRID 2181682 の反応式
O1[C:5]2[CH:6]=[CH:7][C:8]([C:10](OC)=O)=C[C:4]=2[CH:3]=[CH:2]1.[C:14]([O-:17])(O)=O.[Na+].[Br:19]Br.C([O-])([O-])=O.[K+].[K+]>C(Cl)Cl>[CH3:10][C:8]1[O:17][C:14]2[CH:2]=[CH:3][CH:4]=[CH:5][C:6]=2[C:7]=1[Br:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 11430Potassium CarbonateHCID 24408BromineHCID 516892Sodium BicarbonateHCID 12674941Methyl 1-benzofuran-5-carboxylate

生成物 1

HCID 115140063-Bromo-2-methyl-1-benzofuran収率 75%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Methyl benzofuran-5-carboxylate (1.74 g, 9.9 mmol) is dissolved in CH2Cl2 (50 mL), layered with saturated NaHCO3 (75 mL) using very slow magnetic stirring so that the two layers are not mixed and treated with Br2 (3.1 mL, 59.1 mmol). The bi-phasic mixture is stirred slowly for 2 h, then vigorously for 1 h. The layers are separated and the aqueous layer is extracted with CH2Cl2 (2×50 mL). The organics are dried (Na2SO4) and concentrated under reduced pressure without heat. The residue is dissolved in MeOH (100 mL), treated with K2CO3 (8.17 g, 59.1 mmol) and stirred at RT for 18 h. The mixture is concentrated to dryness, partitioned between 50% saturated NaHCO3 (75 mL) and EtOAc (2×75 mL) and the organics are dried (Na2SO4) and concentrated in vacuo. The crude material (2.21 g) is adsorbed onto silica gel (4.5 g) chromatographed over 90 g slurry-packed silica gel, eluting with 8% EtOAc/hexane then 15% EtOAc/hexane. The appropriate fractions are combined and concentrated to afford 1.88 g (75%) of methyl 3-bromo-1-benzofuran as a white solid. 1H NMR (300 MHz, CDCl3): δ 3.99, 7.55, 7.74, 8.11, 8.31 ppm.

後処理

  1. additionare not mixed
  2. stirringThe bi-phasic mixture is stirred slowly for 2 h
  3. customThe layers are separated
  4. extractionthe aqueous layer is extracted with CH2Cl2 (2×50 mL)
  5. dry with materialThe organics are dried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. temperaturewithout heat
  8. dissolutionThe residue is dissolved in MeOH (100 mL)
  9. stirringstirred at RT for 18 h
  10. concentrationThe mixture is concentrated to dryness
  11. custompartitioned between 50% saturated NaHCO3 (75 mL) and EtOAc (2×75 mL)
  12. dry with materialthe organics are dried (Na2SO4)
  13. concentrationconcentrated in vacuo
  14. customchromatographed over 90 g slurry-packed silica gel
  15. washeluting with 8% EtOAc/hexane
  16. concentrationconcentrated

出典と根拠

ORDレコード
ord-a9816272ace9401084383231913760ad
出典データセット
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06894042B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート