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Benzyl Chloride → Methyl 3-benzyl-4-iodobenzoate

HRID 1361090
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HRID 1361090 반응식
[CH2:1](Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O[C:10]1[CH:11]=[C:12]([CH:17]=[CH:18][C:19]=1[I:20])[C:13]([O:15][CH3:16])=[O:14].C(=O)([O-])[O-].[K+].[K+]>C(C(C)=O)C>[CH2:1]([C:10]1[CH:11]=[C:12]([CH:17]=[CH:18][C:19]=1[I:20])[C:13]([O:15][CH3:16])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7503Benzyl ChlorideHCID 11430Potassium CarbonateHCID 10378812Methyl 3-hydroxy-4-iodobenzoate

생성물 1

HCID 66971745Methyl 3-benzyl-4-iodobenzoate수율 105.5%

시약·촉매·용매 1

HCID 6569Methyl Ethyl Ketone용매

실험 절차

47 ml (411 mmol) of benzyl chloride are added to a solution of 104 g (374 mmol) of methyl 3-hydroxy-4-iodobenzoate and 103 g (748 mmol) of potassium carbonate in 600 ml of methyl ethyl ketone, and the reaction medium is then refluxed for 8 hours. After cooling, the reaction medium is filtered, the precipitate is rinsed with ethyl acetate and the filtrate is evaporated to dryness. The residue is taken up in a mixture of water and ethyl acetate. The organic phase is dried over sodium sulfate, filtered and evaporated. 139 g (100%) of methyl 3-benzyl-4-iodobenzoate are obtained in the form of a white solid.

후처리

  1. temperaturethe reaction medium is then refluxed for 8 hours
  2. temperatureAfter cooling
  3. filtrationthe reaction medium is filtered
  4. washthe precipitate is rinsed with ethyl acetate
  5. customthe filtrate is evaporated to dryness
  6. additionThe residue is taken up in a mixture of water and ethyl acetate
  7. dry with materialThe organic phase is dried over sodium sulfate
  8. filtrationfiltered
  9. customevaporated

출처 및 근거

ORD 기록
ord-bc02926280b744a2ac545cce46f0c0d0
출처 데이터셋
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07879907B2

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