Acetic Acid → HCID 86644233, compound

HRID 451331Notes

Reaction equation

HRID 451331 reaction equation
[Cl:1][CH2:2][C:3](=O)[CH2:4]C(OCC)=O.[C:11]([OH:14])(=[O:13])[CH3:12].[CH:15]([NH2:18])([CH3:17])[CH3:16].[C:19]1(C)C=CC=C[CH:20]=1>C(O)C>[Cl:1][CH2:2][C:3]([NH:18][CH:15]([CH3:17])[CH3:16])=[CH:4][CH2:12][C:11]([O:14][CH2:19][CH3:20])=[O:13]

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 1140TolueneHCID 6363IsopropylamineHCID 69484Ethyl 4-chloroacetoacetate

Product 1

HCID 86644233HCID 86644233, compoundYield 82%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a solution of 100 g of ethyl 4-chloroacetoacetate in 300 ml of toluene and 100 ml of ethanol are added 7 ml of acetic acid. At 10° C.-30° C., with cooling, 38.3 g of isopropylamine are added dropwise. Subsequently, the mixture is stirred at room temperature for 5 h and the solvent is removed under reduced pressure at temperatures of down to 35° C. 141.8 g of ethyl 4-chloro-3-(isopropylamino)but-2-enecarboxylate are obtained in a purity of 70% (this corresponds to 82% yield).

Workup

  1. temperatureAt 10° C.-30° C., with cooling
  2. customthe solvent is removed under reduced pressure at temperatures of down to 35° C

Sources & evidence

ORD record
ord-b0c5612ae01443a784d6c26227c8f731
Source dataset
uspto-grants-2013_07
Patent number
US08487112B2

Reaction notes

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