1-Bromo-3-chloropropane → 1-[4-((3-Chloropropyl)thio]-3-methoxyphenyl]ethanone

HRID 1069312Notes

Reaction equation

HRID 1069312 reaction equation
[CH3:1][C:2]([C:4]1[CH:10]=[C:9]([O:11][CH3:12])[C:7](=[S:8])[CH2:6][CH:5]=1)=[O:3].C(=O)([O-])[O-].[K+].[K+].Br[CH2:20][CH2:21][CH2:22][Cl:23].C1CCCCC1>CC(C)=O>[Cl:23][CH2:22][CH2:21][CH2:20][S:8][C:7]1[CH:6]=[CH:5][C:4]([C:2](=[O:3])[CH3:1])=[CH:10][C:9]=1[O:11][CH3:12]

Participants

6

Reactant 4

HCID 80061-Bromo-3-chloropropaneHCID 8078CyclohexaneHCID 11430Potassium CarbonateHCID 219601011-(4-Thio-3-methoxyphenyl)ethanone

Product 1

HCID 102442711-[4-((3-Chloropropyl)thio]-3-methoxyphenyl]ethanone

Reagents, catalysts & solvents 1

HCID 180AcetoneSolvent2×

Procedure

A mixture of 1-(4thio-3-methoxyphenyl)ethanone (10.0 g, 54.9 mmol), potassium carbonate (9.0 g 65.1 mmol), and acetone (100 ml) was stirred at reflux under nitrogen for 30 minutes. The reaction was cooled to ambient temperature and a solution of 1-bromo-3-chloropropane (6.5 ml, 9.5 g, 60.4 mmol) dissolved in acetone (25 ml) was dripped into the reaction. After complete addition, the reaction was carried to substantial completion, the reaction mixture was filtered and the resulting filter cake was washed with acetone. The filtrate was concentrated to provide an amber oil. A small sample was solidified by trituration with hot cyclohexane to provide 1-[4-[(3-chloropropyl)thio]-3-methoxyphenyl]ethanone as a yellow solid, 11.7 g, m.p.=53-55° C.

Workup

  1. temperatureat reflux under nitrogen for 30 minutes
  2. customwas dripped into the reaction
  3. additionAfter complete addition
  4. filtrationthe reaction mixture was filtered
  5. filtrationthe resulting filter cake
  6. washwas washed with acetone
  7. concentrationThe filtrate was concentrated
  8. customto provide an amber oil

Sources & evidence

ORD record
ord-7ab0e4f433b145ea9aa10d081e49bb3c
Source dataset
uspto-grants-2001_06
Patent number
US06251907B1

Reaction notes

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