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Phenethyl bromide → 5-Chloro-2-(2-phenylethoxy)benzaldehyde

HRID 2397054
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인쇄 미리보기

반응식

HRID 2397054 반응식
[Cl:1][C:2]1[CH:9]=[C:6]([CH:7]=[O:8])[C:5]([OH:10])=[CH:4][CH:3]=1.Br[CH2:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>C(#N)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:10][CH2:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[C:6]([CH:9]=1)[CH:7]=[O:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7666Phenethyl bromideHCID 124815-Chloro-salicylaldehyde

생성물 1

HCID 189868805-Chloro-2-(2-phenylethoxy)benzaldehyde

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

5 g of 5-chlorosalicylaldehyde was dissolved in 300 ml of acetonitrile. After adding 41.48 g of potassium fluoride/alumina (neutral) (2:3) and 17.45 ml of (2-bromoethyl)benzene, the resulting mixture was stirred at room temperature for 63 hours. Then the potassium fluoride/alumina was removed by filtration under sucking and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent; n-hexane:ethyl acetate=10:1) and recrystallized from isopropyl ether to give 5.58 g of 5-chloro-2-(2-phenylethoxy)benzaldehyde.

후처리

  1. customThen the potassium fluoride/alumina was removed by filtration
  2. customthe solvent was evaporated under reduced pressure
  3. customThe residue was purified by silica gel column chromatography (developing solvent; n-hexane:ethyl acetate=10:1)
  4. customrecrystallized from isopropyl ether

출처 및 근거

ORD 기록
ord-8f86f6282e874c0281feba95f40f1f40
출처 데이터셋
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05495046

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