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

Magnesium Carbonate → Ethyl 2-propylthiazole-5-carboxylate

HRID 1659120
ノート
印刷プレビュー

反応式

HRID 1659120 の反応式
[C:1]([NH2:6])(=[S:5])[CH2:2][CH2:3][CH3:4].[CH:7]([CH:9](Cl)[C:10]([O:12][CH2:13][CH3:14])=[O:11])=O.C(=O)([O-])[O-].[Mg+2]>O1CCOCC1>[CH2:2]([C:1]1[S:5][C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:7][N:6]=1)[CH2:3][CH3:4]
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

5

反応物 3

HCID 11029Magnesium CarbonateHCID 118030Ethyl (chloroformyl)acetateHCID 12454243Butanethioamide

生成物 1

HCID 21413783Ethyl 2-propylthiazole-5-carboxylate収率 79.5%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
60 °C

実験手順

A mixture of 38 g of thiobutyramide, 54.2 g of ethyl 2-formyl-2-chloro-acetate, 185 ml of dioxane and 22 g of magnesium carbonate was heated for 4 hours at 60°C and the precipitate formed was removed by filtration. The dioxane was distilled from the filtrate and the residue was taken up in 665 ml of a 1-1 ethyl ether-water mixture. The ether phase was recovered by decantation and was washed with aqueous 10% hydrochloric acid solution and then with water until the wash waters were neutral, dried over magnesium sulfate and distilled to dryness. The residue was distilled to obtain 57 g of ethyl 2-n-propylthiazol-5-carboxylate boiling at 95°-106°C under 0.5 mm Hg.

後処理

  1. customthe precipitate formed
  2. customwas removed by filtration
  3. distillationThe dioxane was distilled from the filtrate
  4. customThe ether phase was recovered by decantation
  5. washwas washed with aqueous 10% hydrochloric acid solution
  6. dry with materialdried over magnesium sulfate
  7. distillationdistilled to dryness
  8. distillationThe residue was distilled

出典と根拠

ORDレコード
ord-5de2a2621d6d43db9fa6194c20c4e9d3
出典データセット
uspto-grants-1976_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US03966950

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