Dichloromethane → HCID 19900858, compound

HRID 1029706Notes

Reaction equation

HRID 1029706 reaction equation
[CH3:1][S:2][CH2:3][C:4]1[O:5][CH:6]=[CH:7][CH:8]=1.[C:9](=[O:12])([O-:11])[O-].[Na+].[Na+].[CH2:15](Cl)Cl.BrBr>CO>[CH3:1][S:2][CH2:3][C:4]1([O:5][CH3:6])[CH:8]=[CH:7][CH:9]([O:12][CH3:15])[O:11]1

Participants

6

Conditions

Temperature
-20 °C

Procedure

A mixture of 2-methylthiomethyl furan (23.3 g, 0.182 mole), anhydrous sodium carbonate (32.16 g, 0.303 mole), methylene chloride (40 mL) and absolute methanol (40 mL) was cooled to -20° C. under nitrogen atmosphere. A solution of bromine (24.32 g, 0.152 mole) in 60 mL absolute methanol was added over a period of one hour. The reaction mixture was stirred for another 4 hours and filtered by suction. The filtrate was stirred with anhydrous potassium carbonate (10 g--1 hour) and filtered. The solvents were removed on the rotatory evaporator and methylene chloride (100 mL) was added. The organic solution was dried over anhydrous sodium sulfate, filtered and the solvent was removed on the rotatory evaporator. The residue was distilled under reduced pressure to give 16.51 g (57%) of pure product, bp 66°-68° C. (0.4 mm Hg), nD =1.4860.

Workup

  1. filtrationfiltered by suction
  2. stirringThe filtrate was stirred with anhydrous potassium carbonate (10 g--1 hour)
  3. filtrationfiltered
  4. customThe solvents were removed on the rotatory evaporator and methylene chloride (100 mL)
  5. additionwas added
  6. dry with materialThe organic solution was dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customthe solvent was removed on the rotatory evaporator
  9. distillationThe residue was distilled under reduced pressure

Sources & evidence

ORD record
ord-3425b9dd5c794e258fedf736888fdbdb
Source dataset
uspto-grants-1992_04
Patent number
US05102909

Reaction notes

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