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Potassium Iodide → Methyl 4-(2-iodoethyl)benzoate

HRID 1512196
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반응식

HRID 1512196 반응식
Cl[CH2:2][CH2:3][C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=1.[I-:14].[K+]>C(#N)C>[I:14][CH2:2][CH2:3][C:4]1[CH:13]=[CH:12][C:7]([C:8]([O:10][CH3:11])=[O:9])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4875Potassium IodideHCID 22098587Methyl 4-(2-chloroethyl)benzoate

생성물 1

HCID 22639144Methyl 4-(2-iodoethyl)benzoate

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

70 g (352.4 mmol) of methyl 4-(2-chloroethyl)benzoate [CAS Reg. No. 65787-72-6] and 146.2 g (880.9 mmol) of potassium iodide are suspended in 800 ml of acetonitrile and stirred under reflux for three days. After the reaction has gone to completion, the reaction solution is cooled and filtered, and the filtrate is evaporated to dryness under reduced pressure. The resulting residue is purified by flash chromatography on silica gel (mobile phase: petroleum ether/ethyl acetate 30:1→20:1). This gives 101 g (348.3 mmol, 98.8% of theory) of a yellowish oil.

후처리

  1. temperatureunder reflux for three days
  2. temperaturethe reaction solution is cooled
  3. filtrationfiltered
  4. customthe filtrate is evaporated to dryness under reduced pressure
  5. customThe resulting residue is purified by flash chromatography on silica gel (mobile phase: petroleum ether/ethyl acetate 30:1→20:1)

출처 및 근거

ORD 기록
ord-73622908ca18476080d1858fe349cd55
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08217063B2

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