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

Nitromethane → Methyl 4-formyl-2-methoxybenzoate

HRID 59315
ノート
印刷プレビュー

反応式

HRID 59315 の反応式
C[O-:2].[Na+].[N+](C)([O-])=O.Br[CH2:9][C:10]1[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[C:12]([O:20][CH3:21])[CH:11]=1>CO>[CH:9]([C:10]1[CH:19]=[CH:18][C:13]([C:14]([O:16][CH3:17])=[O:15])=[C:12]([O:20][CH3:21])[CH:11]=1)=[O:2]
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 3

HCID 6375NitromethaneHCID 10942334Sodium MethoxideHCID 11288398Methyl 4-(bromomethyl)-2-methoxybenzoate

生成物 1

HCID 18510332Methyl 4-formyl-2-methoxybenzoate収率 641%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

To a solution of sodium methoxide (0.260 g, 4.82 mmol) in methanol (200 mL) was added nitromethane (4.03 g, 11.58 mmol) under nitrogen atmosphere and the reaction mixture was stirred and reflux for 30 minutes. Methyl 4-(bromomethyl)-2-methoxybenzoate (10.00 g, 9.65 mmol) in methanol was added and the reaction mixture was refluxed for 7-8 h. The reaction mass was concentrated and diluted with CHCl3. The diluted reaction mass was washed with 2N NaOH solution. The organic layer was dried over anhydrous sodium sulphate and concentrated to afford 6.00 g of desired product. 1H NMR (300 MHz, DMSO d6): δ 3.83 (m, 6H), 7.36 (d, J=6.6 Hz, 2H), 7.79 (d, J=7.8 Hz, 1H), 10.04 (s, 1H).

後処理

  1. temperaturereflux for 30 minutes
  2. temperaturethe reaction mixture was refluxed for 7-8 h
  3. concentrationThe reaction mass was concentrated
  4. additiondiluted with CHCl3
  5. customThe diluted reaction mass
  6. washwas washed with 2N NaOH solution
  7. dry with materialThe organic layer was dried over anhydrous sodium sulphate
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-8135556d67a7411db9c242346f41abc8
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09439890B2

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