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

Methylhydrazine → HCID 19917896、化合物

HRID 1755875
ノート
印刷プレビュー

反応式

HRID 1755875 の反応式
[OH:1][NH:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][O:12][N:13]2C(=O)C3=CC=CC=C3C2=O)=[CH:7][CH:6]=1)=[O:4].CNN>CN(C)C=O>[NH2:13][O:12][CH2:11][C:8]1[CH:7]=[CH:6][C:5]([C:3]([NH:2][OH:1])=[O:4])=[CH:10][CH:9]=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 2

HCID 6061MethylhydrazineHCID 19917987HCID 19917987、化合物

生成物 1

HCID 19917896HCID 19917896、化合物収率 66.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
0 °C

実験手順

N-Hydroxy-α-(phthalimidooxy)-p-toluamide (10.0 g) (32 mmol) are suspended in 80 ml of absolute dimethylformamide and treated at -5° C. with 1.86 g (40 mmol) of methylhydrazine. After stirring at room temperature for 2.5 hours 40 ml of solvent are distilled off in a high vacuum at room temperature. Insoluble material is filtered off and washed with a small amount of dimethylformamide. The mother liquor and wash solution are treated with 70 ml of ethanol. After stirring at 0° C. for 1/2 hour the precipitated crystalline product is filtered off under suction and washed with a small amount of ethanol. After drying in a high vacuum at room temperature there are obtained 3.9 g of α-(aminooxy)-N-hydroxy-p-toluamide as white crystals of m.p. 145° C. (dec.).

後処理

  1. distillationare distilled off in a high vacuum at room temperature
  2. filtrationInsoluble material is filtered off
  3. washwashed with a small amount of dimethylformamide
  4. washThe mother liquor and wash solution
  5. additionare treated with 70 ml of ethanol
  6. filtrationis filtered off under suction
  7. washwashed with a small amount of ethanol
  8. customAfter drying in a high vacuum at room temperature

出典と根拠

ORDレコード
ord-b80996b928ea4478a4fb2720268fc8f8
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05438052

反応ノート

読み込み中…

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