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

Diazomethane → Methyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetate

HRID 971703
ノート
印刷プレビュー

反応式

HRID 971703 の反応式
[N+](=[CH2:3])=[N-].[CH3:4][C:5]1[N:9]=[C:8]([CH2:10][C:11]([OH:13])=[O:12])[O:7][N:6]=1>C(OCC)C.O>[CH3:4][C:5]1[N:9]=[C:8]([CH2:10][C:11]([O:13][CH3:3])=[O:12])[O:7][N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 9550DiazomethaneHCID 213130182-(3-Methyl-1,2,4-oxadiazol-5-yl)acetic acid

生成物 1

HCID 54453761Methyl 2-(3-methyl-1,2,4-oxadiazol-5-yl)acetate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of an excess of diazomethane in diethyl ether was added to a stirred, cold (about 2° C.) solution of 14 g of 3-methyl-1,2,4-oxadiazol-5-yl-acetic acid in 500 ml of diethyl ether. After the initially vigorous evolution of nitrogen was finished, the solution was concentrated on the steam bath to about 250 ml. The solution was washed three times with 100 ml of water and the wash waters were combined, adjusted to a pH of 9.0 and were extracted with diethyl ether to obtain the part of the product which dissolved in water during the washings. The combined ethereal extracts were filtered through a water repelling paper filter and then were evaporated in vacuo. After keeping the residue for 1 hour at 8 mm the residual oil weighed 14.8 g. The yellow oil was distilled at 0.4-0.5 mm and the collected fraction with a boiling point 70°-71° C. to obtain 12.3 g of methyl 3-methyl-1,2,4-oxadiazol-5-yl-acetate with a refractive index nD25 =1.4472.

後処理

  1. concentrationthe solution was concentrated on the steam bath to about 250 ml
  2. washThe solution was washed three times with 100 ml of water
  3. extractionwere extracted with diethyl ether
  4. customto obtain the part of the product which
  5. filtrationThe combined ethereal extracts were filtered through a water repelling paper
  6. filtrationfilter
  7. customwere evaporated in vacuo
  8. customfor 1 hour
  9. distillationThe yellow oil was distilled at 0.4-0.5 mm

出典と根拠

ORDレコード
ord-fd4f19c45b1d42878442d5569fdcd58b
出典データセット
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04160829

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