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

Hydrochloric Acid → 2,3-Dimethyl-6-nitrobenzylamine

HRID 979524
ノート
印刷プレビュー

反応式

HRID 979524 の反応式
[CH3:1][C:2]1[C:9]([CH3:10])=[CH:8][CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:3]=1[C:4]#[N:5].Cl>O1CCCC1>[CH3:1][C:2]1[C:9]([CH3:10])=[CH:8][CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:3]=1[CH2:4][NH2:5]
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 313Hydrochloric AcidHCID 135090072,3-Dimethyl-6-nitrobenzonitrile

生成物 1

HCID 150650752,3-Dimethyl-6-nitrobenzylamine収率 95%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

A solution of borane-tetrahydrofuran complex (94.6 g, 1.1 mole) in tetrahydrofuran (1100 mL) was added dropwise to a stirred solution of 2,3-dimethyl-6-nitrobenzonitrile (96 g, 0.55 mole) in dry tetrahydrofuran (650 mL) maintained under an atmosphere of argon. After stirring overnight, 10% hydrochloric acid solution (1300 mL) was added dropwise and the mixture heated to reflux. After 30 minutes, the tetrahydrofuran was distilled off, the residue filtered to remove insoluble material and the filtrate made basic with concentrated ammonium hydroxide solution (350 mL). The mixture was extracted with diethyl ether (2×500 mL), the combined extracts washed with water (2×400 mL), dried over potassium carbonate and concentrated to afford 2,3-dimethyl-6-nitrobenzyl amine (93.85 g, 95%) as an oil used without further purification as follows.

後処理

  1. temperaturemaintained under an atmosphere of argon
  2. temperaturethe mixture heated to reflux
  3. waitAfter 30 minutes
  4. distillationthe tetrahydrofuran was distilled off
  5. filtrationthe residue filtered
  6. customto remove insoluble material
  7. extractionThe mixture was extracted with diethyl ether (2×500 mL)
  8. washthe combined extracts washed with water (2×400 mL)
  9. dry with materialdried over potassium carbonate
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-f71e9624de2c48b39ff2d559f0bd44ea
出典データセット
uspto-grants-1987_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04668686

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