Ethyl bromoacetate → HCID 86609217, compound

HRID 1694709Notes

Reaction equation

HRID 1694709 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([S:8]([CH2:11][CH3:12])(=[O:10])=[O:9])[CH:5]=[CH:4][C:3]=1[C:13]1[C:14]([OH:20])=[CH:15][CH:16]=[C:17]([Cl:19])[CH:18]=1.[CH2:21]([O:23][C:24](=[O:27])[CH2:25]Br)[CH3:22]>>[Cl:1][C:2]1[CH:7]=[C:6]([S:8]([CH2:11][CH3:12])(=[O:9])=[O:10])[CH:5]=[CH:4][C:3]=1[C:13]1[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:14]=1[O:20][CH2:25][C:24]([O:23][CH2:21][CH3:22])=[O:27]

Participants

3

Reactant 2

HCID 7748Ethyl bromoacetateHCID 67279695HCID 67279695, compound

Product 1

HCID 86609217HCID 86609217, compound

Procedure

The subtitle compound was prepared by the method of example 1 step (i) using the product from step (iv) and ethylbromoacetate. Yield 2.23 g

Sources & evidence

ORD record
ord-6739d841978d46e58be5d79d43ae1ca6
Source dataset
uspto-grants-2012_04
Patent number
US08158820B2

Reaction notes

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