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

Chloroacetaldehyde → HCID 486298、化合物

HRID 1073208
ノート
印刷プレビュー

反応式

HRID 1073208 の反応式
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.Cl[CH2:12][CH:13]=O>C(O)CCC>[N:1]1[CH:12]=[CH:13][N:6]2[C:5]3[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=3[S:3][C:2]=12
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 2

HCID 33ChloroacetaldehydeHCID 8706Benzo(d)thiazol-2-amine

生成物 1

HCID 486298HCID 486298、化合物

試薬・触媒・溶媒 1

HCID 2631-Butanol溶媒

実験手順

In 250 ml of n-butanol were heated 10.0 g of 2-aminobenzothiazole and 30 ml of 40% chloroacetaldehyde at 90° C. for 27 hours. After the solvent was removed (evaporated to dryness), the residue was crystallized in isopropanol-acetone to give 6.2 g of imidazo[2,1-b]benzothiazole. Subsequently, 4.0 g of the crystals were added to a mixture of 50 ml of dry dimethylformamide and 3.5 ml of phosphorus oxychloride followed by heating at 60° C. for 3 hours and at 75° C. for 6 hours. After completion of the reaction, the reaction mixture was poured onto ice water. After neutralizing with potassium carbonate, the mixture was extracted with ethyl acetate. The ethyl acetate was removed to give 2.2 g of 3-formylimidazo[2,1-b]benzothiazole. The thus obtained formyl compound, 1.3 g, was added to 20 ml of ethanol and furthermore 0.1 g of sodium borohydride was added to the mixture while stirring under ice cooling. After stirring at the same temperature for 10 minutes, the solvent was removed. The residue was treated with water and filtered to give 1.2 g of the title compound.

後処理

  1. customAfter the solvent was removed
  2. custom(evaporated to dryness)
  3. customthe residue was crystallized in isopropanol-acetone

出典と根拠

ORDレコード
ord-7ad41aeef0ca473698b3d41cf086a3d4
出典データセット
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04968708

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