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Diethylene Glycol → 2-Benzyl-5-bromo-1-benzofuran

HRID 268386
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HRID 268386 반응식
[C:1]([C:9]1[O:10][C:11]2[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:12]=2[CH:13]=1)(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.NN.C(O)COCCO.[OH-].[K+]>O>[CH2:1]([C:9]1[O:10][C:11]2[CH:17]=[CH:16][C:15]([Br:18])=[CH:14][C:12]=2[CH:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8117Diethylene GlycolHCID 9321HydrazineHCID 14797Potassium HydroxideHCID 801609(5-Bromo-1-benzofuran-2-yl)(phenyl)methanone

생성물 1

HCID 227689092-Benzyl-5-bromo-1-benzofuran

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 42.2 g. (0.14 mol.) of 2-benzoyl-5-bromobenzofuran and 35 ml. of 98% hydrazine in 70 ml. of diethylene glycol is warmed for a few minutes on a steam bath. Then 23.3 g. of potassium hydroxide is added and the reaction mixture is refluxed for 2 hours. After cooling, water is added to the mixture and the resulting aqueous solution is extracted with benzene. The extract is washed with water, 10% aqueous hydrochloric acid and water, dried (MgSO4) and concentrated to yield 2-benzyl-5-bromobenzofuran.

후처리

  1. additionA mixture of 42.2 g
  2. temperaturethe reaction mixture is refluxed for 2 hours
  3. temperatureAfter cooling
  4. extractionthe resulting aqueous solution is extracted with benzene
  5. washThe extract is washed with water, 10% aqueous hydrochloric acid and water
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated

출처 및 근거

ORD 기록
ord-5b72da4bd9df435b8e7ce97f9d0098c5
출처 데이터셋
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03947470

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