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

HRID 361471
Notes
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Reaction equation

HRID 361471 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 174Ethylene GlycolSolvent

Procedure

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, 2 H), 0.55 (m, 2 H), 2.50 (d, 2 H), 7.14 (d, 2 H), 7.41 (d, 2 H); mass spectrum (EI+) 210 (M.)+.

Workup

  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

Sources & evidence

ORD record
ord-a955da66795b45b6b9a20c28ddf95d80
Source dataset
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05866568

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes