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

Methanol → (4-Nitro-1,2-phenylene)dimethanol

HRID 386616
ノート
印刷プレビュー

反応式

HRID 386616 の反応式
[N+:1]([C:4]1[CH:5]=[C:6]([C:13](O)=[O:14])[C:7](=[CH:11][CH:12]=1)[C:8](O)=[O:9])([O-:3])=[O:2].CO>C1COCC1>[N+:1]([C:4]1[CH:12]=[CH:11][C:7]([CH2:8][OH:9])=[C:6]([CH2:13][OH:14])[CH:5]=1)([O-:3])=[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

4

反応物 2

HCID 887MethanolHCID 691211,2-Benzenedicarboxylic acid, 4-nitro-

生成物 1

HCID 11019518(4-Nitro-1,2-phenylene)dimethanol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

A solution of 4-nitrophthalic acid (40 g, 189.5 mmol) in THF (500 mL) was added dropwise over 1.5 h to a solution of borane-THF complex (1 M, 490 mL, 490 mmol), keeping the reaction temperature between 0° C. and 5° C. After the addition, the reaction mixture was allowed to warm slowly to ambient temperature and stirred for 18 h. MeOH (100 mL) was added carefully and the precipitated solid dissolved. The mixture was concentrated in vacuo to about 500 mL, cooled to 0° C., and 10 N NaOH was added to adjust the pH to 10-11. This mixture was extracted with EtOAc (3×600 mL) and the combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated in vacuo to give the title compound. MS: m/z=207 (M−OH+CH3CN).

後処理

  1. customthe reaction temperature between 0° C. and 5° C
  2. additionAfter the addition
  3. dissolutionthe precipitated solid dissolved
  4. concentrationThe mixture was concentrated in vacuo to about 500 mL
  5. temperaturecooled to 0° C.
  6. addition10 N NaOH was added
  7. extractionThis mixture was extracted with EtOAc (3×600 mL)
  8. washthe combined organic layers were washed with brine
  9. dry with materialdried over Na2SO4
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-a22aa8ebe6094a94917e5c64b22d9c71
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08372859B2

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