Ethyl bromoacetate → HCID 85939545, compound

HRID 2049308Notes

Reaction equation

HRID 2049308 reaction equation
[CH2:1]([O:3][C:4](=[O:7])[CH2:5]Br)[CH3:2].[S:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[C:13]([C:15]1[CH:20]=[CH:19][C:18]([OH:21])=[C:17]([Br:22])[CH:16]=1)=[O:14]>>[CH2:1]([O:3][C:4](=[O:7])[CH2:5][O:21][C:18]1[CH:19]=[CH:20][C:15]([C:13](=[O:14])[C:9]2[S:8][CH:12]=[CH:11][CH:10]=2)=[CH:16][C:17]=1[Br:22])[CH3:2]

Participants

3

Reactant 2

HCID 7748Ethyl bromoacetateHCID 23469770HCID 23469770, compound

Product 1

HCID 85939545HCID 85939545, compoundYield 95%

Procedure

This ester was prepared with 95% yield by reaction of ethylbromoacetate with (3-bromo-4-hydroxyphenyl) (2-thienyl) ketone. The product was an oil.

Sources & evidence

ORD record
ord-0f5596d443704678b52716b5badf0999
Source dataset
uspto-grants-1980_04
Patent number
US04197309

Reaction notes

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