Ethyl diazoacetate → HCID 178468948, compound
Reaction equation
[CH3:1][C:2](=[O:5])[C:3]#[CH:4].[CH2:6]([O:8][C:9](=[O:13])[CH:10]=[N+:11]=[N-:12])[CH3:7]>O>[CH2:6]([O:8][C:9]([C:10]1[CH:4]=[C:3]([C:2](=[O:5])[CH3:1])[NH:12][N:11]=1)=[O:13])[CH3:7]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
But-3-yn-2-one (Int 5, 1 eq) and diazo-acetic acid ethyl ester (Int 6, 1.1 eq) are added to a solution of InCl3 (0.2 eq) in water and stirred for 30 min at room temperature. After overnight stirring at room temperature, the mixture is diluted with water and extracted with EtOAc. The resulting organic phase is dried and evaporated to give the desired product.
Workup
- stirringAfter overnight stirring at room temperature
- extractionextracted with EtOAc
- customThe resulting organic phase is dried
- customevaporated
Sources & evidence
- ORD record
- ord-ebb2cc9e4ff5470eb76d76b2b6eefa5a
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09351955B2
Reaction notes
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