Carbon Dioxide → Methyl 2,2,3,3-tetrafluoro-3-(methylsulfanyl)propanoate

HRID 1632157Notes

Reaction equation

HRID 1632157 reaction equation
[H-].[Na+].[CH3:3][SH:4].[C:5](=[O:7])=O.[F:8][C:9]([F:13])=[C:10]([F:12])[F:11].S([O:19][CH3:20])(OC)(=O)=O>CS(C)=O>[CH3:3][S:4][C:10]([F:12])([F:11])[C:9]([F:13])([F:8])[C:5]([O:19][CH3:20])=[O:7]

Participants

7

Procedure

A slurry of 24 g (0.50 mole) of 50% NaH/mineral oil in 140 ml of dry dimethyl sulfoxide was stirred while 24 g (0.50 mole) of methyl mercaptan was distilled in over a 2 hr. period. The mixture was then stirred until gas evolution became very slow after which the mixture was allowed to stand overnight. The resulting mixture was a thick paste which was diluted with 50 ml of dimethyl sulfoxide and charged into a 400 ml metal tube along with 33 g (0.75 mole) of carbon dioxide and 50 g (0.50 mole) of tetrafluoroethylene. The tube was shaken at 100° for 4 hr. The resulting solution was treated with 69.3 g (0.55 mole) of dimethyl sulfate. After an initial exotherm (maximum temperature, 50°), the mixture was stirred for 3 hr. Product was then removed under vacuum and fractionated to afford 63.9 g (62%) of methyl 3-methylthio-2,2,3,3-tetrafluoropropionate, bp 53° (10 mm, 1.3 kPa), IR (neat): 3020, 2970, and 2860 (satd CH), 1780 (C=O), and 1250-1100 cm-1 (C--F), 1H and 19F NMR agreed with the assigned structure.

Workup

  1. distillationwas distilled in over a 2 hr
  2. additionwas diluted with 50 ml of dimethyl sulfoxide
  3. stirringThe tube was shaken at 100° for 4 hr
  4. stirringAfter an initial exotherm (maximum temperature, 50°), the mixture was stirred for 3 hr
  5. customProduct was then removed under vacuum

Sources & evidence

ORD record
ord-592b946567b840ad9077298a6f9471be
Source dataset
uspto-grants-1984_10
Patent number
US04474700

Reaction notes

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