Ethyl bromoacetate → (4-Acetyl-2-ethyl-3-hydroxy-phenoxy)-acetic acid ethyl ester

HRID 2357043Notes

Reaction equation

HRID 2357043 reaction equation
[CH2:1]([C:3]1[C:4]([OH:13])=[C:5]([C:10](=[O:12])[CH3:11])[CH:6]=[CH:7][C:8]=1[OH:9])[CH3:2].[CH2:14]([O:16][C:17](=[O:20])[CH2:18]Br)[CH3:15]>>[CH2:14]([O:16][C:17](=[O:20])[CH2:18][O:9][C:8]1[CH:7]=[CH:6][C:5]([C:10](=[O:12])[CH3:11])=[C:4]([OH:13])[C:3]=1[CH2:1][CH3:2])[CH3:15]

Participants

3

Reactant 2

HCID 7748Ethyl bromoacetateHCID 212870211-(3-Ethyl-2,4-dihydroxyphenyl)ethanone

Product 1

HCID 67246312(4-Acetyl-2-ethyl-3-hydroxy-phenoxy)-acetic acid ethyl ester

Procedure

1-(3-Ethyl-2,4-dihydroxy-phenyl)-ethanone was treated with 2-bromo-acetic acid ethyl ester and processed as described in the synthesis of example 20a. Yield, 96.89%; mp, 74-75° C.; MS (CI): 267 (M++1).

Workup

  1. customas described in the synthesis of example 20a
  2. customYield
  3. custommp, 74-75° C.

Sources & evidence

ORD record
ord-f5550d46ac7f42a7bad4f61cf3b6f007
Source dataset
uspto-grants-2010_07
Patent number
US07759387B2

Reaction notes

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