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Diethylene Glycol → 2-Butyl-5-chloro-1-benzofuran

HRID 1283655
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HRID 1283655 반응식
[C:1]([C:6]1[O:7][C:8]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:9]=2[CH:10]=1)(=O)[CH2:2][CH2:3][CH3:4].NN.C(O)COCCO.[OH-].[K+]>O>[CH2:1]([C:6]1[O:7][C:8]2[CH:14]=[CH:13][C:12]([Cl:15])=[CH:11][C:9]=2[CH:10]=1)[CH2:2][CH2:3][CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8117Diethylene GlycolHCID 9321HydrazineHCID 14797Potassium HydroxideHCID 215104891-(5-Chloro-1-benzofuran-2-yl)butan-1-one

생성물 1

HCID 138150732-Butyl-5-chloro-1-benzofuran

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 31.5 g. (0.14 mol.) of 2-butyryl-5-chlorobenzofuran and 35 ml. of 98% hydrazine in 70 ml. of diethylene glycol was warmed for a few minutes on a steam bath. Then 23.3 g. of potassium hydroxide was added and the reaction mixture was refluxed for two hours. After cooling, water was added to the mixture and the resulting aqueous solution was extracted with benzene. The extract was washed with water, 10% aqueous hydrochloric acid and water, dried (MgSO4) and concentrated in vacuo to yield 2-n-butyl-5-chlorobenzofuran, b.p. 70°-75° (10-15 mm.).

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후처리

  1. additionA mixture of 31.5 g
  2. temperaturethe reaction mixture was refluxed for two hours
  3. temperatureAfter cooling
  4. extractionthe resulting aqueous solution was extracted with benzene
  5. washThe extract was washed with water, 10% aqueous hydrochloric acid and water
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-026b91de298840b9855cd8b147cb307c
출처 데이터셋
uspto-grants-1976_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US03975537

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