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

Methanol → HCID 178496795、化合物

HRID 1067920
ノート
印刷プレビュー

反応式

HRID 1067920 の反応式
CO[C:3](OC)=[N:4][NH:5][C:6]([O:8][CH3:9])=[O:7].[CH3:12][NH2:13].[CH3:14][OH:15]>>[CH3:14][O:15][CH2:12][NH:13][CH:3]=[N:4][NH:5][C:6]([O:8][CH3:9])=[O:7]
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 3

HCID 887MethanolHCID 6329MethylamineHCID 10986557HCID 10986557、化合物

生成物 1

HCID 178496795HCID 178496795、化合物

実験手順

4.77 g (25.0 mmol) of methyl N′-dimethoxymethylenehydrazinecarboxylate (85% pure) were admixed with 15.3 g of a 51% strength solution of methylamine (250 mmol) in methanol, and the mixture was stirred at room temperature for 3 days. The orange-red solution was concentrated under reduced pressure to remove excess methylamine. This gave crude methyl N′-(methoxymethylaminomethylene)hydrazinecarboxylate which was then taken up in methanol (15 ml) and, with 4.95 g (27.5 mmol) of sodium methoxide solution (30% in methanol), heated to 50° C. After 3 h 50 min, the reaction mixture was cooled to room temperature, neutralized using 2N HCl and concentrated under reduced pressure. The residue was taken up in water (6 ml) and stored overnight in a fridge. The colourless crystals were filtered off, washed with cold water and dried under reduced pressure. This gave 1.70 g (52.7%) of 5-methoxy-4-methyl-2,4-dihydro-1,2,4-triazol-3-one in the form of a colourless solid. Melting point 146-148° C.

後処理

  1. concentrationThe orange-red solution was concentrated under reduced pressure
  2. customto remove excess methylamine

出典と根拠

ORDレコード
ord-f60190baf6944d9e859a35d28be50ca6
出典データセット
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06248900B1

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