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Potassium Hydroxide → 1-Bromo-4-(cyclopropylmethyl)benzene

HRID 1384256
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HRID 1384256 반응식
[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([Br:12])=[CH:8][CH:7]=2)=O)[CH2:3][CH2:2]1.O.NN.[OH-].[K+]>C(O)CO>[Br:12][C:9]1[CH:10]=[CH:11][C:6]([CH2:4][CH:1]2[CH2:2][CH2:3]2)=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14797Potassium HydroxideHCID 24654Hydrazine hydrate (1:1)HCID 813944-Bromophenyl cyclopropyl ketone

생성물 1

HCID 116513971-Bromo-4-(cyclopropylmethyl)benzene수율 49.2%

시약·촉매·용매 1

HCID 174Ethylene Glycol용매

실험 절차

4-Bromophenyl cyclopropyl ketone (5.63 g), hydrazine monohydrate (2.5 ml) and potassium hydroxide (3.33 g) were added to ethylene glycol (25 ml) and the mixture heated to reflux for 1 hour. The reaction mixture was cooled and partitioned between water (20 ml) and ethyl acetate (30 ml) and the organic layer was separated. The aqueous layer was extracted with ethyl acetate (30 ml) and the combined organic phases were washed with 2M hydrochloric acid (15 ml) and water (15 ml) then dried (MgSO4) and evaporated. The residue was purified by chromatography on a Mega Bond Elut column, eluting with hexane to give 1-bromo-4-(cyclopropylmethyl)benzene (2.6 g); 1H NMR (CDCl3): 0.2 (m, 2H), 0.55 (m, 2H), 2.50 (d, 2H), 7.14 (d, 2H), 7.41 (d, 2H); mass spectrum (EI+) 210 (M.)+.

후처리

  1. temperaturethe mixture heated
  2. temperatureto reflux for 1 hour
  3. temperatureThe reaction mixture was cooled
  4. custompartitioned between water (20 ml) and ethyl acetate (30 ml)
  5. customthe organic layer was separated
  6. extractionThe aqueous layer was extracted with ethyl acetate (30 ml)
  7. washthe combined organic phases were washed with 2M hydrochloric acid (15 ml) and water (15 ml)
  8. dry with materialthen dried (MgSO4)
  9. customevaporated
  10. customThe residue was purified by chromatography on a Mega Bond Elut column
  11. washeluting with hexane

출처 및 근거

ORD 기록
ord-b0dc0e857a85423a8741b4e64ca2367c
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06258817B1

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