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

HRID 594844
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HRID 594844 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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).

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후처리

  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

출처 및 근거

ORD 기록
ord-b8e34cdff52e4f46a153d378166175f3
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242973B2

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