Diethyl Malonate → HCID 23037015, compound

HRID 1709103Notes

Reaction equation

HRID 1709103 reaction equation
[C:1]([C:3]1[CH:21]=[CH:20][C:6]([O:7][C:8]2[CH:19]=[CH:18][C:11]([O:12]C(C)C(Cl)=O)=[CH:10][CH:9]=2)=[CH:5][CH:4]=1)#[N:2].[C:22]([O:30][CH2:31][CH3:32])(=[O:29])[CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25].[Mg].C(OCC)(=O)CC(OCC)=O>CCOCC>[CH2:31]([O:30][C:22](=[O:29])[CH:23]([O:12][C:11]1[CH:18]=[CH:19][C:8]([O:7][C:6]2[CH:20]=[CH:21][C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)=[CH:9][CH:10]=1)[C:24]([O:26][CH2:27][CH3:28])=[O:25])[CH3:32]

Participants

5

Procedure

A mixture of 30 g of 2-[4'-(4"-cyano-phenoxy)-phenoxy]-propionyl chloride and 30 ml of ether is added dropwise to a 35% etheral solution of magnesium diethyl malonate prepared from 17.6 g of diethyl malonate. The addition of the acid chloride having been completed the reaction mixture is heated to boiling for an hour and worked up as described in Example 1. Thus 30 g of the desired compound are obtained in the form of a viscous oil which solidifies on standing and melts at 42°-46° C. Yield 72%.

Workup

  1. temperatureis heated
  2. waitto boiling for an hour

Sources & evidence

ORD record
ord-bb2efed75c3445ff85f0f5bb8d113201
Source dataset
uspto-grants-1990_08
Patent number
US04948420

Reaction notes

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