3,4-Difluoroanisole → 1-Fluoro-4-methoxy-2-methylsulfanylbenzene

HRID 1827953Notes

Reaction equation

HRID 1827953 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1F.[CH3:11][S-:12].[Na+]>CN(C)C=O.O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH3:9])=[CH:4][C:3]=1[S:12][CH3:11]

Participants

5

Conditions

Temperature
60 °C

Procedure

1,2-Difluoro-4-methoxy-benzene (100 mg, 0.69 mmol) and sodium methanethiolate (148 mg, 2.08 mmol) were dissolved in N,N-dimethylformamide (2 mL) and the reaction mixture stirred at 60° C. for 18 hours. Additional sodium methanethiolate (99 mg, 139 mmol) was added and the reaction mixture heated to 100° C. for 18 hours. The reaction mixture was diluted with water and extracted with ether (×2). The ether extracts were washed with water (×2), dried over magnesium sulphate and concentrated in vacuo. The residue was taken up in pentane:ether 1:1 mixture (2 mL) and filtered through a plug of silica in a pipette, washing through with pentane:ether 1:1 mixture (5 mL). The reaction mixture was concentrated in vacuo to yield the title product as a colourless oil, 135 mg.

Workup

  1. temperaturethe reaction mixture heated to 100° C. for 18 hours
  2. extractionextracted with ether (×2)
  3. washThe ether extracts were washed with water (×2)
  4. dry with materialdried over magnesium sulphate
  5. concentrationconcentrated in vacuo
  6. filtrationfiltered through a plug of silica in a pipette
  7. washwashing through with pentane:ether 1:1 mixture (5 mL)
  8. concentrationThe reaction mixture was concentrated in vacuo

Sources & evidence

ORD record
ord-8818197c2223438481abe590664ae904
Source dataset
uspto-grants-2006_06
Patent number
US07056934B2

Reaction notes

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