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2-Phenyl-benzofuran → 3-(3-Methyl-4-methoxybenzoyl)-2-phenylbenzofuran

HRID 268379
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HRID 268379 반응식
[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:5](Cl)=[O:6].[C:13]1([C:19]2[O:20][C:21]3[CH:27]=[CH:26][CH:25]=[CH:24][C:22]=3[CH:23]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>C(=S)=S>[CH3:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[C:5]([C:23]1[C:22]2[CH:24]=[CH:25][CH:26]=[CH:27][C:21]=2[O:20][C:19]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 35179362-Phenyl-benzofuranHCID 210929304-Methoxy-3-methylbenzoyl chloride

생성물 1

HCID 214353193-(3-Methyl-4-methoxybenzoyl)-2-phenylbenzofuran

시약·촉매·용매 1

HCID 6348Carbon Disulfide용매

실험 절차

To a cooled, stirred solution of 10.8 g. (0.058 mol.) of 3-methyl-4-methoxybenzoic acid chloride and 9.6 g. (0.054 mol.) of 2-phenylbenzofuran in 40 ml. of carbon disulfide is added dropwise over a 20 minute interval 28.2 g. (0.108 mol.) of stannic chloride. After addition, the reaction mixture is warmed to ambient temperature and stirred for 2 hours. The mixture is then poured onto 100 ml. of ice-water and stirred for 1 hour. The solvent is removed, and the product extracted into chloroform and the extracts are washed with water, dried (Na2SO4) and concentrated under reduced pressure to give 3-(3-methyl-4-methoxybenzoyl)-2-phenylbenzofuran.

후처리

  1. additionAfter addition
  2. stirringstirred for 2 hours
  3. additionThe mixture is then poured onto 100 ml
  4. customThe solvent is removed
  5. extractionthe product extracted into chloroform
  6. washthe extracts are washed with water
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-462a09f066324439b8f5a7ca85494815
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03947470

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