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

HRID 223613Notes

Reaction equation

HRID 223613 reaction equation
[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]

Participants

5

Reactant 3

HCID 949N,N-DimethylanilineHCID 3146661,1,3-Tribromo-2-propanoneHCID 130920372,2,2-Trichloroethyl carbamothioylcarbamate

Product 1

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

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-fca4fbac2e874a7f976e66dab7fc0125
Source dataset
uspto-grants-1982_10
Patent number
US04355160

Reaction notes

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