1-Bromo-3-chloropropane → HCID 12016522, compound

HRID 1167837Notes

Reaction equation

HRID 1167837 reaction equation
[CH:1]1([C:4]([C:6]2[CH:11]=[CH:10][C:9]([OH:12])=[CH:8][CH:7]=2)=[O:5])[CH2:3][CH2:2]1.C([O-])([O-])=O.[K+].[K+].Br[CH2:20][CH2:21][CH2:22][Cl:23]>CC(=O)CC>[Cl:23][CH2:22][CH2:21][CH2:20][O:12][C:9]1[CH:8]=[CH:7][C:6]([C:4]([CH:1]2[CH2:2][CH2:3]2)=[O:5])=[CH:11][CH:10]=1

Participants

5

Reactant 3

HCID 80061-Bromo-3-chloropropaneHCID 11430Potassium CarbonateHCID 10515124-cyclopropanecarbonylphenol

Product 1

HCID 12016522HCID 12016522, compound

Reagents, catalysts & solvents 1

HCID 6569Methyl Ethyl KetoneSolvent

Procedure

Cyclopropyl(4-hydroxyphenyl)methanone (10 g, 61.7 mmol), K2CO3 (12.7 g, 91.9 mmol), and 1-bromo-3-chloropropane (10.74 g, 68.2 mmol) in 2-butanone (100 mL) were refluxed for 24 hours, allowed to cool to ambient temperature, filtered, and concentrated. The residue was heated at 40° C. under reduced pressure for three hours to provide the title compound of sufficient purity for subsequent use without further purification (13.25 g, 90%).

Workup

  1. filtrationfiltered
  2. concentrationconcentrated
  3. temperatureThe residue was heated at 40° C. under reduced pressure for three hours

Sources & evidence

ORD record
ord-f5b34f7ab31f4d6cbeba28290d6be927
Source dataset
uspto-grants-2003_09
Patent number
US06620839B2

Reaction notes

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