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

Sodium → 2-Amino-4-(2,2-dichlorovinyl)-6-methoxypyrimidine

HRID 3909
ノート
印刷プレビュー

反応式

HRID 3909 の反応式
[NH2:1][C:2]1[N:7]=[C:6](Cl)[CH:5]=[C:4]([CH:9]=[C:10]([Cl:12])[Cl:11])[N:3]=1.[CH3:13][O-:14].[Na+].[Na]>CO>[NH2:1][C:2]1[N:3]=[C:4]([CH:9]=[C:10]([Cl:12])[Cl:11])[CH:5]=[C:6]([O:14][CH3:13])[N:7]=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 3

HCID 5360545SodiumHCID 10942334Sodium MethoxideHCID 201535042-Amino-4-chloro-6-(2,2-dichlorovinyl)pyrimidine

生成物 1

HCID 201535032-Amino-4-(2,2-dichlorovinyl)-6-methoxypyrimidine

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

22.0 Parts of 2-amino-4-chloro-6-(2,2-dichlorovinyl)pyrimidine was dissolved in 500 parts of dry methanol and stirred whilst a solution of sodium methoxide, prepared by dissolving 4.6 parts of sodium in 200 parts of dry methanol, was added dropwise, over 30 minutes at ambient temperature. The resulting solution was stirred for 4 hours by which time all the starting material had been consumed. The product was precipitated by the addition of water, filtered and dried. The solid obtained was purified by chromatography on silica using diethyl ether as eluent. Final purification was effected by recrystallisation from carbon tetrachloride to give 2-amino-4-(2,2-dichlorovinyl)-6-methoxypyrimidine m.p. 90°-91° C.

後処理

  1. customprepared
  2. additionwas added dropwise, over 30 minutes at ambient temperature
  3. customhad been consumed
  4. customThe product was precipitated by the addition of water
  5. filtrationfiltered
  6. customdried
  7. customThe solid obtained
  8. customwas purified by chromatography on silica
  9. customFinal purification
  10. customwas effected by recrystallisation from carbon tetrachloride

出典と根拠

ORDレコード
ord-c486bd8087ef4bc39cbd7955c7ea7c4c
出典データセット
uspto-grants-1988_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04723006

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