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

N'-Benzylidene-4-methylbenzene-1-sulfonohydrazide → Benzene, (diazomethyl)-

HRID 428440
ノート
印刷プレビュー

反応式

HRID 428440 の反応式
S([NH:11][N:12]=[CH:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)(C1C=CC(C)=CC=1)(=O)=O.C[O-].[Na+]>CO>[C:14]1([CH:13]=[N+:12]=[N-:11])[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
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 277551N'-Benzylidene-4-methylbenzene-1-sulfonohydrazideHCID 10942334Sodium Methoxide

生成物 1

HCID 136601Benzene, (diazomethyl)-

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

In an oven-dried round bottom flask was placed benzaldehyde tosylhydrazone (1.15 g, 4.2 mmol), followed by 4.3 mL of a 1.0 M solution of sodium methoxide in methanol (2.3 g Na metal dissolved in absolute methanol and diluted to 100 mL). The mixture was swirled until all the contents dissolved. Most of the solvent was removed via rotary evaporation and the last traces of solvent by evacuation of the flask under high vacuum for 2 hours. The solid obtained was subjected to a Kugelrohr distillation at 215° C. and 200 millitorr for 1 hour. At 68-70° C., the title compound, as a red oil, was collected in a receiver flask in a quantitative yield.

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

後処理

  1. customIn an oven-dried round bottom flask was placed
  2. dissolutiondissolved
  3. customMost of the solvent was removed via rotary evaporation
  4. customThe solid obtained
  5. distillationwas subjected to a Kugelrohr distillation at 215° C.
  6. wait200 millitorr for 1 hour
  7. customAt 68-70° C., the title compound, as a red oil, was collected in a receiver flask in a quantitative yield

出典と根拠

ORDレコード
ord-7d1b90adda91403ca5d87e3b3516a405
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06313290B1

反応ノート

読み込み中…