RU1779240C - Способ получени дикетена - Google Patents
Способ получени дикетенаInfo
- Publication number
- RU1779240C RU1779240C SU904742731A SU4742731A RU1779240C RU 1779240 C RU1779240 C RU 1779240C SU 904742731 A SU904742731 A SU 904742731A SU 4742731 A SU4742731 A SU 4742731A RU 1779240 C RU1779240 C RU 1779240C
- Authority
- RU
- Russia
- Prior art keywords
- diketene
- sulfur
- ketene
- dimerization
- sulfur dioxide
- Prior art date
Links
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims description 18
- 238000002360 preparation method Methods 0.000 title claims description 3
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims abstract description 17
- CCGKOQOJPYTBIH-UHFFFAOYSA-N ethenone Chemical compound C=C=O CCGKOQOJPYTBIH-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000003112 inhibitor Substances 0.000 claims abstract description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 12
- 238000006471 dimerization reaction Methods 0.000 claims description 9
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- 238000000197 pyrolysis Methods 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 abstract description 2
- 239000003153 chemical reaction reagent Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 description 7
- 239000000047 product Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 230000000737 periodic effect Effects 0.000 description 2
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 101000916532 Rattus norvegicus Zinc finger and BTB domain-containing protein 38 Proteins 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007233 catalytic pyrolysis Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 1
- ABTOQLMXBSRXSM-UHFFFAOYSA-N silicon tetrafluoride Chemical compound F[Si](F)(F)F ABTOQLMXBSRXSM-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D315/00—Heterocyclic compounds containing rings having one oxygen atom as the only ring hetero atom according to more than one of groups C07D303/00 - C07D313/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/87—Preparation of ketenes or dimeric ketenes
- C07C45/89—Preparation of ketenes or dimeric ketenes from carboxylic acids, their anhydrides, esters or halides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/87—Preparation of ketenes or dimeric ketenes
- C07C45/90—Separation; Purification; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH30/89A CH676361A5 (enExample) | 1989-01-05 | 1989-01-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU1779240C true RU1779240C (ru) | 1992-11-30 |
Family
ID=4177765
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU904742731A RU1779240C (ru) | 1989-01-05 | 1990-01-03 | Способ получени дикетена |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4999438A (enExample) |
| EP (1) | EP0377438B1 (enExample) |
| JP (1) | JP2805930B2 (enExample) |
| CN (1) | CN1025558C (enExample) |
| CA (1) | CA2007048C (enExample) |
| CH (1) | CH676361A5 (enExample) |
| DE (1) | DE59004261D1 (enExample) |
| RU (1) | RU1779240C (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4239117A1 (de) * | 1992-11-20 | 1994-05-26 | Wacker Chemie Gmbh | Verfahren zur Isolierung von reinem Diketen unter Rückgewinnung von Wertstoffen |
| CN114160191B (zh) * | 2021-12-02 | 2023-07-14 | 万华化学集团股份有限公司 | 一种催化裂化催化剂及其制备方法与应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE700218C (de) * | 1937-03-14 | 1940-12-16 | Consortium Elektrochem Ind | Verfahren zur Darstellung von Diketen |
| DE1240847B (de) * | 1963-08-02 | 1967-05-24 | Basf Ag | Verfahren zur Herstellung von Diketen aus Keten in Gegenwart eines Loesungsmittels und eines sauren Dimerisierungskatalysators |
| CH421080A (de) * | 1963-11-29 | 1966-09-30 | Lonza Ag | Verfahren zur Verminderung der Harzbildung bei der Herstellung und Lagerung von Diketen |
| US4377490A (en) * | 1979-06-29 | 1983-03-22 | Sumitomo Chemical Company, Limited | Adhesive composition |
| US4364913A (en) * | 1981-09-24 | 1982-12-21 | American Cyanamid Company | HNCO Manufacture by adiabatic air oxidation of HCN |
| US4389386A (en) * | 1981-09-24 | 1983-06-21 | American Cyanamid Company | HNCO Manufacture by catalytic oxidation of HCN with a Pd doped Ag catalyst |
-
1989
- 1989-01-05 CH CH30/89A patent/CH676361A5/de not_active IP Right Cessation
- 1989-12-27 CN CN89109706.6A patent/CN1025558C/zh not_active Expired - Fee Related
- 1989-12-28 JP JP1338864A patent/JP2805930B2/ja not_active Expired - Lifetime
-
1990
- 1990-01-02 DE DE90100031T patent/DE59004261D1/de not_active Expired - Fee Related
- 1990-01-02 EP EP90100031A patent/EP0377438B1/de not_active Expired - Lifetime
- 1990-01-03 US US07/460,659 patent/US4999438A/en not_active Expired - Fee Related
- 1990-01-03 RU SU904742731A patent/RU1779240C/ru active
- 1990-01-03 CA CA002007048A patent/CA2007048C/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| D.Borrmann в справочнике Houbenweyl Methoden der organixhen chemie. т.7/4. 1968, s.226,228. Патент DE № 1240847, кл. 12021. 1967. Патент DE № 1268625, кл. 12024, 1952 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02221267A (ja) | 1990-09-04 |
| US4999438A (en) | 1991-03-12 |
| DE59004261D1 (de) | 1994-03-03 |
| EP0377438B1 (de) | 1994-01-19 |
| CH676361A5 (enExample) | 1991-01-15 |
| EP0377438A1 (de) | 1990-07-11 |
| CN1043931A (zh) | 1990-07-18 |
| CA2007048A1 (en) | 1990-07-05 |
| CA2007048C (en) | 1999-07-27 |
| CN1025558C (zh) | 1994-08-03 |
| JP2805930B2 (ja) | 1998-09-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH10504563A (ja) | ラクチドの製造方法 | |
| EP0291361A2 (en) | Stabilization of vanadium tetrachloride | |
| US4814505A (en) | Purification of n-vinylformamide | |
| JPH07330659A (ja) | 純粋グレードのアクリル酸の製造方法 | |
| JP2010083780A (ja) | 沸点200℃以上の高沸点成分の分離回収方法およびポリアリーレンスルフィドの製造方法 | |
| RU1779240C (ru) | Способ получени дикетена | |
| US5824195A (en) | Process for distilling crude acrylic silane solution | |
| US4554377A (en) | Production of N-vinyl carboxylic acid amides | |
| US4283524A (en) | Process for polymerization of composition comprising (1) alpha,beta-unsaturated monocarboxylic acid or ammonium salt thereof and (2) ammonia | |
| JPS5848572B2 (ja) | 窒化塩化燐ポリマ−の製造方法 | |
| JP4356120B2 (ja) | 高純度ジアリールカーボネート及びその製造方法 | |
| US3912701A (en) | Olefin polymerization process | |
| JP2004277363A (ja) | アクリルアミドアルカンスルホン酸の精製方法 | |
| JPS6027609A (ja) | 環式ジクロロホスフアゼンの重合法 | |
| EP0283375B1 (fr) | Procédé de préparation de polychlorophosphazène | |
| US4591444A (en) | Process for exhaustively decontaminating perfluoropolyethereal oils | |
| US5476973A (en) | Stable m-vinylphenol composition, and methods of stabilizing and purifying m-vinylphenol | |
| JPH06122661A (ja) | N−ビニルホルムアミドの製造法 | |
| US4188494A (en) | Hydrogen fluoride removal from glycolic acid | |
| RU2144019C1 (ru) | Способ получения пентафторйодэтана | |
| JPH1112230A (ja) | ジフェニルカーボネートの精製方法 | |
| WO2006114432A2 (en) | Method for purifying glycolide | |
| SU379563A1 (ru) | Способ получепия высокомолекулярного алкенилянтарного ангидрида | |
| RU1826974C (ru) | Способ получени олигомерного 1,2-дигидро-2,2,4-триметилхинолина | |
| SU178443A1 (ru) | Способ очистки ацетилена |