Ethyl diazoacetate → HCID 178468948, compound

HRID 2279202Notes

Reaction equation

HRID 2279202 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

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

  1. stirringAfter overnight stirring at room temperature
  2. extractionextracted with EtOAc
  3. customThe resulting organic phase is dried
  4. customevaporated

Sources & evidence

ORD record
ord-64ac089d066f4f2491c281f0c0bbac50
Source dataset
uspto-grants-2015_09
Patent number
US09133210B2

Reaction notes

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