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

Nitric Acid → HCID 178433402、化合物

HRID 614649
ノート
印刷プレビュー

反応式

HRID 614649 の反応式
S(=O)(=O)(O)O.[CH3:6][C:7]1[NH:8][CH:9]=[CH:10][N:11]=1.NC(N)=O.[N+:16]([O-])([OH:18])=[O:17]>O>[CH3:6][C:7]1[NH:8][CH:9]=[C:10]([N+:16]([O-:18])=[O:17])[N:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 944Nitric Acid2 回HCID 1118Sulfuric AcidHCID 1176UreaHCID 127492-Methylimidazole

生成物 1

HCID 178433402HCID 178433402、化合物収率 89%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

A mixture of 330 parts of sulfuric acid (36 percent by weight), 100 parts of 2-methylimidazole, 50 parts of urea, 283 parts of nitric acid (31 percent by weight) and 153 parts of water is kept for 6.5 hours in a distillation vessel, equipped with a stirrer, at from 123° to 130° C. During the reaction, 20 parts of 30 percent strength by weight nitric acid distill off. The reaction mixture is then diluted with a 3.5-fold volume of water whilst cooling and is neutralized to pH 3-4 with ammonia solution. The 2-methyl-4-nitroimidazole which separates out is centrifuged off, washed, dried and recrystallized from water. 138 parts of 2-methyl-4-nitroimidazole (89.0% of theory) of melting point 145°-146° C. are obtained.

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. customequipped with a stirrer, at from 123° to 130° C
  2. distillationdistill off
  3. additionThe reaction mixture is then diluted with a 3.5-fold volume of water
  4. temperaturewhilst cooling
  5. washwashed
  6. customdried
  7. customrecrystallized from water

出典と根拠

ORDレコード
ord-3a44af94cf034985a40c8d859e21ede1
出典データセット
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04145553

反応ノート

読み込み中…