Methanol → HCID 23236268, compound

HRID 1657953Notes

Reaction equation

HRID 1657953 reaction equation
[F:1][C:2]([F:11])=[C:3]([C:7]([F:10])([F:9])[F:8])[C:4](F)=[O:5].[CH3:12][OH:13].[F-].[Na+].[OH2:16]>CCOCC>[F:1][C:2]([F:11])([O:13][CH3:12])[CH:3]([C:7]([F:10])([F:9])[F:8])[C:4]([OH:16])=[O:5]

Participants

6

Procedure

A solution of 50 g (0.28 mol) of perfluoromethacryloyl fluoride in 100 ml of ether was stirred at 0°C while 9.0 g (0.28 mol) of methanol was added at a rate sufficient to keep the reaction mixture near 20°C. When the addition was complete, 100 g of anhydrous NaF was added, and the mixture was stirred while 5.4 g (0.30 mol) of water was added. The temperature was not allowed to go above 35°C. After having stood overnight, the reaction mixture was filtered and distilled. It was necessary to keep the pot temperature below 70°C to avoid excessive etching. 3,3-Difluoro-3-methoxy-2-trifluoromethylpropionic acid was obtained as 22.1 g (38%) of distillate, bp 45°C (0.5 mm); ir (neat): 3.25 (broad, OH), 5.72 (C=O), 7.5-9 μ (CF, COC); nmr (CCl4): 1H at 11.8 (singlet, 1, OH), 3.83 (sextet (quartet, JHF = 7.5 Hz, into triplets, JHF = 7.5 Hz), 1, CH), and 3.67 ppm (singlet, 3, OCH3); 19F at -65.1 ppm (triplet, JFF = 10.5 Hz, into doublets, JHF = 7.5 Hz, 3, CF3) and 14 lines from overlapping center lines of an AB pattern at -4233 Hz and -4247 Hz (both quartets, JFF = 10.5 Hz, into doublets, JHF = 7.5 Hz, 2, CF2).

Workup

  1. additionwas added at a rate sufficient
  2. customnear 20°C
  3. additionWhen the addition
  4. additionwas added
  5. customto go above 35°C
  6. filtrationthe reaction mixture was filtered
  7. distillationdistilled
  8. customthe pot temperature below 70°C

Sources & evidence

ORD record
ord-677cffeb1d13478fb08d3b11249124d0
Source dataset
uspto-grants-1976_06
Patent number
US03962325

Reaction notes

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