Dimethyl Sulfide → 2-Fluoro-1-methoxymethoxy-4-methylsulfanyl benzene

HRID 1792504Notes

Reaction equation

HRID 1792504 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:9][O:10][CH3:11])=[C:4]([F:12])[CH:3]=1.C([Li])CCC.[CH3:18][S:19]C.[Cl-].[NH4+]>O1CCCC1.O>[F:12][C:4]1[CH:3]=[C:2]([S:19][CH3:18])[CH:7]=[CH:6][C:5]=1[O:8][CH2:9][O:10][CH3:11]

Participants

7

Conditions

Temperature
0 °C

Procedure

5 g of 4-bromo-2-fluoro-1-methoxymethoxybenzene was dissolved in 50 mL anhydrous tetrahydrofuran, and 13.4 mL n-butyl lithium (1.59 M hexane solution) was added dropwise thereto at −70° C. After the mixture was stirred for 1 hour, 2.1 ml dimethyl sulfide was added dropwise thereto and stirred at −70° C. for 1 hour, and after the temperature of the reaction solution was raised to 0° C., the solution was stirred for 1 hour. An aqueous saturated ammonium chloride solution was added thereto, the mixture was stirred for 30 minutes, and water added to the mixture which was then extracted with ethyl acetate. The extract was dried over sodium sulfate and purified by silica gel chromatography (hexane/ethyl acetate) to give 3.67 g of 2-fluoro-1-methoxymethoxy-4-methylsulfanyl benzene. 4 mL solution of 4 N hydrogen chloride in ethyl acetate was added to this reaction product and left for 1 hour. Water was added to the product which was then extracted with ethyl acetate and purified by silica gel chromatography (hexane/ethyl acetate) to give 1.01 g of the title compound as a colorless oil.

Workup

  1. customat −70° C
  2. stirringstirred at −70° C. for 1 hour
  3. stirringthe solution was stirred for 1 hour
  4. stirringthe mixture was stirred for 30 minutes
  5. extractionwas then extracted with ethyl acetate
  6. dry with materialThe extract was dried over sodium sulfate
  7. custompurified by silica gel chromatography (hexane/ethyl acetate)

Sources & evidence

ORD record
ord-55b308ab717d4f438e10bc8c641a8222
Source dataset
uspto-grants-2006_07
Patent number
US07074801B1

Reaction notes

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