RU2010150091A - METHOD FOR PRODUCING PERFLUOROETHYLISOPROPYL KETONE IN AN IDEAL EXPRESSION REACTOR - Google Patents

METHOD FOR PRODUCING PERFLUOROETHYLISOPROPYL KETONE IN AN IDEAL EXPRESSION REACTOR Download PDF

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RU2010150091A
RU2010150091A RU2010150091/04A RU2010150091A RU2010150091A RU 2010150091 A RU2010150091 A RU 2010150091A RU 2010150091/04 A RU2010150091/04 A RU 2010150091/04A RU 2010150091 A RU2010150091 A RU 2010150091A RU 2010150091 A RU2010150091 A RU 2010150091A
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RU
Russia
Prior art keywords
producing
activated carbon
perfluoroethylisopropyl
ketone
hexafluoropropene
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RU2010150091/04A
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Russian (ru)
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RU2460717C2 (en
Inventor
Валерий Георгиевич Барабанов (RU)
Валерий Георгиевич Барабанов
Юрий Иванович Бабенко (RU)
Юрий Иванович Бабенко
Татьяна Алексеевна Биспен (RU)
Татьяна Алексеевна Биспен
Андрей Сергеевич Васильев (RU)
Андрей Сергеевич Васильев
Виктор Александрович Маталин (RU)
Виктор Александрович Маталин
Дмитрий Дмитриевич Молдавский (RU)
Дмитрий Дмитриевич Молдавский
Иван Михайлович Феничев (RU)
Иван Михайлович Феничев
Original Assignee
Федеральное государственное унитарное предприятие "Российский научный центр "Прикладная химия" (RU)
Федеральное государственное унитарное предприятие "Российский научный центр "Прикладная химия"
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Application filed by Федеральное государственное унитарное предприятие "Российский научный центр "Прикладная химия" (RU), Федеральное государственное унитарное предприятие "Российский научный центр "Прикладная химия" filed Critical Федеральное государственное унитарное предприятие "Российский научный центр "Прикладная химия" (RU)
Priority to RU2010150091/04A priority Critical patent/RU2460717C2/en
Publication of RU2010150091A publication Critical patent/RU2010150091A/en
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Publication of RU2460717C2 publication Critical patent/RU2460717C2/en

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Abstract

1. Способ получения перфторэтилизопропил кетона взаимодействием оксида гексафторпропена и гексафторпропена, отличающийся тем, что способ проводят в реакторе идеального вытеснения без применения растворителя, в присутствии катализатора CsF, нанесенного на активированный уголь, при температуре 100-150°С и давлении 0-0,24 МПа. ! 2. Способ по п.1, отличающийся тем, что в качестве катализатора используют фторид цезия, нанесенный на активированный уголь. 1. The method of producing perfluoroethylisopropyl ketone by the interaction of hexafluoropropene oxide and hexafluoropropene, characterized in that the method is carried out in an ideal displacement reactor without the use of a solvent, in the presence of a CsF catalyst supported on activated carbon, at a temperature of 100-150 ° C and a pressure of 0-0.24 MPa ! 2. The method according to claim 1, characterized in that cesium fluoride supported on activated carbon is used as a catalyst.

Claims (2)

1. Способ получения перфторэтилизопропил кетона взаимодействием оксида гексафторпропена и гексафторпропена, отличающийся тем, что способ проводят в реакторе идеального вытеснения без применения растворителя, в присутствии катализатора CsF, нанесенного на активированный уголь, при температуре 100-150°С и давлении 0-0,24 МПа.1. The method of producing perfluoroethylisopropyl ketone by the interaction of hexafluoropropene oxide and hexafluoropropene, characterized in that the method is carried out in an ideal displacement reactor without the use of a solvent, in the presence of a CsF catalyst supported on activated carbon, at a temperature of 100-150 ° C and a pressure of 0-0.24 MPa 2. Способ по п.1, отличающийся тем, что в качестве катализатора используют фторид цезия, нанесенный на активированный уголь. 2. The method according to claim 1, characterized in that cesium fluoride supported on activated carbon is used as a catalyst.
RU2010150091/04A 2010-12-06 2010-12-06 Method of producing perfluoroethylisopropyl ketone in plug-flow reactor RU2460717C2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
RU2010150091/04A RU2460717C2 (en) 2010-12-06 2010-12-06 Method of producing perfluoroethylisopropyl ketone in plug-flow reactor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
RU2010150091/04A RU2460717C2 (en) 2010-12-06 2010-12-06 Method of producing perfluoroethylisopropyl ketone in plug-flow reactor

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RU2010150091A true RU2010150091A (en) 2012-06-20
RU2460717C2 RU2460717C2 (en) 2012-09-10

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RU2010150091/04A RU2460717C2 (en) 2010-12-06 2010-12-06 Method of producing perfluoroethylisopropyl ketone in plug-flow reactor

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116178123A (en) * 2022-12-09 2023-05-30 天津长芦新材料研究院有限公司 Fluoridation liquid and preparation method thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SU569554A1 (en) * 1975-10-08 1977-08-25 Предприятие П/Я Г-4567 Method of preparing perfluorated ketones
SU698289A1 (en) * 1978-05-24 1985-02-23 Предприятие П/Я Г-4567 Method of obtaining perfluorethylisopropylketone
AU6223600A (en) * 1999-07-20 2001-02-05 3M Innovative Properties Company Use of fluorinated ketones in fire extinguishing compositions
US6540930B2 (en) * 2001-04-24 2003-04-01 3M Innovative Properties Company Use of perfluoroketones as vapor reactor cleaning, etching, and doping gases

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN116178123A (en) * 2022-12-09 2023-05-30 天津长芦新材料研究院有限公司 Fluoridation liquid and preparation method thereof

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RU2460717C2 (en) 2012-09-10

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