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

Dimethyl Sulfate → 2,3-Dimethoxy-6-nitrobenzaldehyde

HRID 652593
ノート
印刷プレビュー

反応式

HRID 652593 の反応式
[K].[OH:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([N+:13]([O-:15])=[O:14])[C:4]=1[CH:5]=[O:6].[C:16](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CN(C=O)C>[CH3:16][O:2][C:3]1[C:10]([O:11][CH3:12])=[CH:9][CH:8]=[C:7]([N+:13]([O-:15])=[O:14])[C:4]=1[CH:5]=[O:6]
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 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 867411922-Hydroxy-3-methoxy-6-nitrobenzaldehyde potassium salt

生成物 1

HCID 71721272,3-Dimethoxy-6-nitrobenzaldehyde

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Potassium salt from Procedure 5 (396 g) was slurried with DMF (8 l) and added to a 1 l flask containing 800 g potassium carbonate. Dimethyl sulfate (420 ml) was added in portions at 60° over 1 hour and the reaction was stirred at 60° overnight. The K2CO3 was washed with acetone and the washings were added to the distillation residue and again solvent was removed in vacuo. The dry residue was treated with water (1 l) and extracted with CH2Cl2. The extracts were dried, evaporated, and the product was crystallized from methanol to afford the product, (335 g, 94%) mp 109°-111° C.

後処理

  1. additionadded to a 1 l flask
  2. washThe K2CO3 was washed with acetone
  3. additionthe washings were added to the distillation residue and again solvent
  4. customwas removed in vacuo
  5. additionThe dry residue was treated with water (1 l)
  6. extractionextracted with CH2Cl2
  7. customThe extracts were dried
  8. customevaporated
  9. customthe product was crystallized from methanol
  10. customto afford the product, (335 g, 94%) mp 109°-111° C.

出典と根拠

ORDレコード
ord-9c3f3f838afb471c9830b74c270466ec
出典データセット
uspto-grants-1987_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04672116

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