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Toluene → HCID 178423709、化合物

HRID 1047653
ノート
印刷プレビュー

反応式

HRID 1047653 の反応式
[N-:1]=[N+:2]=[N-:3].[Na+].[C:5]1(C)[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[C:11]1[CH:18]=[CH:17][CH:16]=[CH:15][C:12]=1[C:13]#[N:14].[C:20]1(C)C=CC=CC=1>>[CH3:20][C:9]1[CH:10]=[CH:5][C:6]([C:11]2[CH:18]=[CH:17][CH:16]=[CH:15][C:12]=2[C:13]2[NH:14][N:3]=[N:2][N:1]=2)=[CH:7][CH:8]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1140TolueneHCID 33557Sodium AzideHCID 112177752-(2-methylphenyl)benzonitrile

生成物 1

HCID 178423709HCID 178423709、化合物

反応条件

温度
100 °C

実験手順

A 20 ml flask is dried under argon and then charged with 7 ml of diisobutylaluminium fluoride (1 molar in hexane) followed by 5 ml of toluene and 455 mg of NaN3 (7 mmol). After stirring the suspension for 4 hours at room temperature 966 mg of solid ortho-tolylbenzonitrile (OTBN) is added at 0° C. in one portion. The suspension is warmed up to 130° C. (ext. temp.) with an internal temperature of 100° C. After 44 h at 130° C. (ext. temp.) the conversion is >93%. The reaction mixture was quenched in hydrochloric acid (6 molar). After addition of 10 ml of toluene the layers are separated, the organic layer is washed twice with 20 ml of water, dried over sodium sulfate and evaporated to give a crystalline residue of the product.

後処理

  1. customA 20 ml flask is dried under argon
  2. additioncharged with 7 ml of diisobutylaluminium fluoride (1 molar in hexane)
  3. additionis added at 0° C. in one portion
  4. customThe reaction mixture was quenched in hydrochloric acid (6 molar)
  5. additionAfter addition of 10 ml of toluene the layers
  6. customare separated
  7. washthe organic layer is washed twice with 20 ml of water
  8. dry with materialdried over sodium sulfate
  9. customevaporated
  10. customto give a crystalline residue of the product

出典と根拠

ORDレコード
ord-35cd4033b06c4bdca35969908b8719cc
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08569528B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート