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Canadian application, no grantCanada

Epoxidation process for manufacture of olefin oxide and alcohol

CA 2101006 A1 · Owner: Texaco Chemical Inc. · Inventors: Keating, Kenneth Patrick; Marquis, Edward Thomas; Mueller, Mark Allan

CIPO record

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Abstract From the Canadian patent

An epoxidation reaction wherein: an olefin and an organic hydroperoxide preferably, propylene and, tertiary butyl hydroperoxide are reacted in a primary reaction zone in a liquid phase with an organic solvent, preferably tertiary butyl alcohol in the presence of a soluble molybdenum catalyst at a ratio of propylene to tertiary butyl hydroperoxide of from about 0.9:1 to about 3:1 at a reaction temperature, from about 100°C to about 140°C and a residence time sufficient to convert about 85 to 95% of the tertiary butyl hydroperoxide and form a primary epoxidation zone reaction product; fractionating in, a primary fractionation zone, the primary zone reaction product into a primary distillate …

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Listed from its CIPO record in Patent Yard's archive of Canadian patents past their term. Its claims, description and drawings are in the CIPO record and on Google Patents, and the Claude kit works from them.

Why it's free to use

  • Filed July 21, 1993. No grant is recorded for it in Canada; had it been granted, its 20-year term would have ended July 21, 2013.
  • A certificate of supplementary protection adds at most two years for a drug, so even that would have ended by July 21, 2015.
  • We check Canadian rights only. A patent in its family in another country could still be in force: check its family on Google Patents.
FiledJuly 21, 1993
GrantedNo grant recorded
Term endedJuly 21, 2013
Patent numberCA 2101006 A1
Classification (IPC)C07D303/04 +2 more

Timeline

Timeline From CIPO dates

1994199619982000200220042006200820102012Application filedJuly 21, 1993Term endedJuly 21, 2013

Sources & verification

Everything on this page comes from the CIPO record linked above. Contains information licensed under the Open Government Licence – Canada.