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1,3-Dibromopropane → HCID 21883826, compound

HRID 604380
Notes
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Reaction equation

HRID 604380 reaction equation
[Br:1][CH2:2][CH2:3][CH2:4]Br.C(=O)([O-])[O-].[K+].[K+].[CH:12]1([C:15]([C:17]2[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][CH:18]=2)=[O:16])[CH2:14][CH2:13]1>CC(C)=O>[Br:1][CH2:2][CH2:3][CH2:4][O:23][C:20]1[CH:19]=[CH:18][C:17]([C:15]([CH:12]2[CH2:13][CH2:14]2)=[O:16])=[CH:22][CH:21]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 80011,3-DibromopropaneHCID 11430Potassium CarbonateHCID 1051512Cyclopropyl(4-hydroxyphenyl)methanone

Product 1

HCID 21883826HCID 21883826, compound

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent2×

Procedure

To a stirred and heated mixture of 1,3-dibromopropane (5 mmol) and potassium carbonate (3.4 mmol) in acetone (40 ml) was added dropwise a solution of 4-cyclopropanecarbonylphenol (5 mmol) in acetone (20 ml). The reaction was allowed to continue overnight. The mixture was filtered hot and the solvent removed under reduced pressure to leave an oil. The oil was purified by column chromatography on silica gel eluting with petroleum ether/ethyl acetate (15:1).

Workup

  1. temperatureheated
  2. filtrationThe mixture was filtered hot
  3. customthe solvent removed under reduced pressure
  4. customto leave an oil
  5. customThe oil was purified by column chromatography on silica gel eluting with petroleum ether/ethyl acetate (15:1)

Sources & evidence

ORD record
ord-c146b9d22db44e2baee94f459391687e
Source dataset
uspto-grants-2011_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07910605B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes