Pyridine → decyl methanesulfinate

HRID 1659170Notes

Reaction equation

HRID 1659170 reaction equation
[CH3:1][S:2](Cl)=[O:3].[CH2:5]([OH:15])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].N1C=CC=CC=1>C(OCC)C>[CH3:1][S:2]([O:15][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[O:3]

Participants

5

Conditions

Temperature
50 °C

Procedure

Into a 50 ml three-necked flask equipped with a magnetic stirrer, thermometer, nitrogen purge and dropping funnel is added 9.9 gms (0.10 moles) of methanesulfinyl chloride. The methane sulfinyl chloride is cooled to -10°C and 17.4 gms (0.11 moles) of decanol is added dropwise while maintaining the temperature of -5° to -10°C. When the addition of the decanol is complete, the reaction mass is warmed to 50°C under 20 mm of vacuum. The resulting product is then cooled and dissolved in 100 ml of diethyl ether admixed with 2 gms. of pyridine. The reaction mass is then extracted with two 10 ml portions of water. A drop of pyridine is added to the ether layer in order to remove additional chloride. In the event that no precipitation occurs the ether layer is then extracted with two 10 ml portions of 3% aqueous hydrochloric acid. The ether layer is then dried over anhydrous sodium sulfate and is then evaporated by means of rotary evaporation yielding an oil which is then subjected to a distillation operation. The resulting product is distilled at 98°C at 0.50-0.65 mm Hg pressure. (Yield 16 gms). GLC, mass spectral and infrared analysis yield the information that the structure of this material is as follows: ##EQU13##

Workup

  1. customInto a 50 ml three-necked flask equipped with a magnetic stirrer
  2. customthermometer, nitrogen purge
  3. temperaturewhile maintaining the temperature of -5° to -10°C
  4. customthe reaction
  5. temperatureThe resulting product is then cooled
  6. extractionThe reaction mass is then extracted with two 10 ml portions of water
  7. additionA drop of pyridine is added to the ether layer in order
  8. customto remove additional chloride
  9. customIn the event that no precipitation
  10. extractionis then extracted with two 10 ml portions of 3% aqueous hydrochloric acid
  11. dry with materialThe ether layer is then dried over anhydrous sodium sulfate
  12. customis then evaporated by means of rotary evaporation
  13. customyielding an oil which
  14. distillationThe resulting product is distilled at 98°C at 0.50-0.65 mm Hg pressure
  15. customyield the information that the structure of this material

Sources & evidence

ORD record
ord-09600bc665ee43868d83b840156ddaa5
Source dataset
uspto-grants-1976_06
Patent number
US03966989

Reaction notes

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