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Potassium Carbonate → 1-(4-Bromo-2-iodophenoxy)-5-chloropentan-2-one

HRID 594844
Notes
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Reaction equation

HRID 594844 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([I:9])[CH:3]=1.Br[CH2:11][C:12](=[O:17])[CH2:13][CH2:14][CH2:15][Cl:16].C([O-])([O-])=O.[K+].[K+]>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:11][C:12](=[O:17])[CH2:13][CH2:14][CH2:15][Cl:16])=[C:4]([I:9])[CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 109245324-Bromo-2-iodophenolHCID 122584391-Bromo-5-chloropentan-2-one

Product 1

HCID 867242361-(4-Bromo-2-iodophenoxy)-5-chloropentan-2-oneYield 46%

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent

Procedure

The mixture of 4-bromo-2-iodophenol (3.30 g, 11.04 mmol), 1-bromo-5-chloropentan-2-one (75% purity, 3.9 g, 14.66 mmol), and K2CO3 (2.3 g, 16.64 mmol) in acetone (66 mL) was stirred for 48 hours at ambient temperature. The insoluble material was removed by filtration and washed with EtOAc. The filtrate was evaporated in vacuo. The residue was purified by silicagel column chromatography (EtOAc-hexane, a linear gradient of EtOAc from 0 to 25%) afforded 1-(4-bromo-2-iodophenoxy)-5-chloropentan-2-one (2.12 g).

Workup

  1. customThe insoluble material was removed by filtration
  2. washwashed with EtOAc
  3. customThe filtrate was evaporated in vacuo
  4. customThe residue was purified by silicagel column chromatography (EtOAc-hexane

Sources & evidence

ORD record
ord-b8e34cdff52e4f46a153d378166175f3
Source dataset
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09242973B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes