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N,N-Dimethylaniline → 2-(beta,beta,beta-Trichloroethoxycarbonyl)amino-4-formylthiazole

HRID 1074240
ノート
印刷プレビュー

反応式

HRID 1074240 の反応式
[Cl:1][C:2]([Cl:12])([Cl:11])[CH2:3][O:4][C:5]([NH:7][C:8]([NH2:10])=[S:9])=[O:6].BrC(Br)C(CBr)=[O:16].CN(C)[C:22]1[CH:27]=CC=C[CH:23]=1>C(O)C>[Cl:12][C:2]([Cl:1])([Cl:11])[CH2:3][O:4][C:5]([NH:7][C:8]1[S:9][CH:23]=[C:22]([CH:27]=[O:16])[N:10]=1)=[O:6]
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 949N,N-DimethylanilineHCID 3146661,1,3-Tribromo-2-propanoneHCID 130920372,2,2-Trichloroethyl carbamothioylcarbamate

生成物 1

HCID 127632072-(beta,beta,beta-Trichloroethoxycarbonyl)amino-4-formylthiazole

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of 10.0 g. of N-(β,β,β-trichloroethoxycarbonyl)thiourea, 12.0 g. of 1,1,3-tribromoacetone and 5.0 g. of dimethylaniline in 100 ml. of ethanol is heated under reflux for 2 hours. After cooling, ethanol is removed under reduced pressure, and the oily residue is dissolved in ethyl acetate. Ethyl acetate layer is washed with water and dried over MgSO4. Ethyl acetate is removed under reduced pressure and the oily residue is dissolved in small quantity of chloroform. From the solution which is allowed to stand at room temperature is obtained 2-(β,β,β-trichloroethoxycarbonyl)amino-4-formylthiazole as a crystalline form. 5.0 g. Melting point: 188°-190° C.

後処理

  1. temperatureunder reflux for 2 hours
  2. temperatureAfter cooling
  3. customethanol is removed under reduced pressure
  4. dissolutionthe oily residue is dissolved in ethyl acetate
  5. washEthyl acetate layer is washed with water
  6. dry with materialdried over MgSO4
  7. customEthyl acetate is removed under reduced pressure
  8. dissolutionthe oily residue is dissolved in small quantity of chloroform
  9. customto stand at room temperature

出典と根拠

ORDレコード
ord-969e7fd14a474c7da56541835b87aa6e
出典データセット
uspto-grants-1990_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04973684

反応ノート

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