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Thiocyanatoacetic acid ethyl ester → HCID 178516935、化合物

HRID 1295455
ノート
印刷プレビュー

反応式

HRID 1295455 の反応式
C([O-])(=O)C.[CH:5]1([NH3+:8])[CH2:7][CH2:6]1.C([O:11][C:12](=O)[CH2:13][S:14][C:15]#[N:16])C>>[CH:5]1([NH:8][C:15]2[S:14][CH2:13][C:12](=[O:11])[N:16]=2)[CH2:7][CH2:6]1
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

3

反応物 2

HCID 21446Thiocyanatoacetic acid ethyl esterHCID 69466131Cyclopropylazanium acetate

生成物 1

HCID 178516935HCID 178516935、化合物収率 37%

反応条件

温度
90 °C

実験手順

A solution of ethyl chloroacetate (20 g, 0.16 mol) and potassium thiocyanate (12.7 g, 0.13 mol) in ethanol (100 ml) was refluxed for 3 h. The solution was filtered and concentrated under reduced pressure to afford 18.7 g of thiocyanato-acetic acid ethyl ester (97%). A mixture of cyclopropylammonium acetate (0.50 g, 4.27 mmol) and thiocyanato-acetic acid ethyl ester (0.62 g, 4.27 mmol) was heated to 90° C. for 3 h, and left at rt overnight. The reaction mixture was partitioned between 6N HCl and dichloromethane. The layers were separated. The aqueous layer was made basic by the addition of 6N ammonium hydroxide, and then concentrated to dryness. The crude was triturated with dichloromethane and the solution separated from the solid by filtration. This solution was dried over sodium sulfate and concentrated to dryness. The crude was purified on a silica gel column with 100% ethyl acetate to afford 2-cyclopropylamino-thiazol-4-one (244 mg, 37%).

後処理

  1. customThe reaction mixture was partitioned between 6N HCl and dichloromethane
  2. customThe layers were separated
  3. additionThe aqueous layer was made basic by the addition of 6N ammonium hydroxide
  4. concentrationconcentrated to dryness
  5. customThe crude was triturated with dichloromethane
  6. customthe solution separated from the solid by filtration
  7. dry with materialThis solution was dried over sodium sulfate
  8. concentrationconcentrated to dryness
  9. customThe crude was purified on a silica gel column with 100% ethyl acetate

出典と根拠

ORDレコード
ord-f5f58b0568cb4d28b4534ecd049a0644
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07241893B2

反応ノート

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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