JPS6224417B2 - - Google Patents
Info
- Publication number
- JPS6224417B2 JPS6224417B2 JP58024848A JP2484883A JPS6224417B2 JP S6224417 B2 JPS6224417 B2 JP S6224417B2 JP 58024848 A JP58024848 A JP 58024848A JP 2484883 A JP2484883 A JP 2484883A JP S6224417 B2 JPS6224417 B2 JP S6224417B2
- Authority
- JP
- Japan
- Prior art keywords
- reaction
- pentafluorobenzonitrile
- fluorinating agent
- pentachlorobenzonitrile
- benzonitrile
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims description 48
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical group [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 claims description 28
- YXWJGZQOGXGSSC-UHFFFAOYSA-N 2,3,4,5,6-pentafluorobenzonitrile Chemical compound FC1=C(F)C(F)=C(C#N)C(F)=C1F YXWJGZQOGXGSSC-UHFFFAOYSA-N 0.000 claims description 20
- INICGXSKJYKEIV-UHFFFAOYSA-N 2,3,4,5,6-pentachlorobenzonitrile Chemical compound ClC1=C(Cl)C(Cl)=C(C#N)C(Cl)=C1Cl INICGXSKJYKEIV-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 16
- 235000003270 potassium fluoride Nutrition 0.000 claims description 14
- 239000011698 potassium fluoride Substances 0.000 claims description 14
- 239000012025 fluorinating agent Substances 0.000 claims description 13
- 239000003444 phase transfer catalyst Substances 0.000 claims description 6
- 229910052784 alkaline earth metal Chemical class 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 150000004673 fluoride salts Chemical class 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 150000001340 alkali metals Chemical class 0.000 claims 2
- 230000002269 spontaneous effect Effects 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 description 27
- 239000002904 solvent Substances 0.000 description 18
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000012452 mother liquor Substances 0.000 description 6
- 229910052801 chlorine Inorganic materials 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 238000009835 boiling Methods 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 150000002222 fluorine compounds Chemical class 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000007086 side reaction Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000002633 crown compound Substances 0.000 description 2
- YSSSPARMOAYJTE-UHFFFAOYSA-N dibenzo-18-crown-6 Chemical compound O1CCOCCOC2=CC=CC=C2OCCOCCOC2=CC=CC=C21 YSSSPARMOAYJTE-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 2
- 230000002194 synthesizing effect Effects 0.000 description 2
- 239000013076 target substance Substances 0.000 description 2
- XEZNGIUYQVAUSS-UHFFFAOYSA-N 18-crown-6 Chemical compound C1COCCOCCOCCOCCOCCO1 XEZNGIUYQVAUSS-UHFFFAOYSA-N 0.000 description 1
- HTKFGTCCOJIUIK-UHFFFAOYSA-N 2,4,6-trifluorobenzonitrile Chemical compound FC1=CC(F)=C(C#N)C(F)=C1 HTKFGTCCOJIUIK-UHFFFAOYSA-N 0.000 description 1
- YOYAIZYFCNQIRF-UHFFFAOYSA-N 2,6-dichlorobenzonitrile Chemical compound ClC1=CC=CC(Cl)=C1C#N YOYAIZYFCNQIRF-UHFFFAOYSA-N 0.000 description 1
- BRCVOCMSJCGQNR-UHFFFAOYSA-N 2-chloro-4,6-difluorobenzonitrile Chemical compound FC1=CC(F)=C(C#N)C(Cl)=C1 BRCVOCMSJCGQNR-UHFFFAOYSA-N 0.000 description 1
- CARZIMSIYVZQDB-UHFFFAOYSA-N 3,5-dichloro-2,4,6-trifluorobenzonitrile Chemical compound FC1=C(Cl)C(F)=C(C#N)C(F)=C1Cl CARZIMSIYVZQDB-UHFFFAOYSA-N 0.000 description 1
- 241000972773 Aulopiformes Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GUNJVIDCYZYFGV-UHFFFAOYSA-K antimony trifluoride Chemical compound F[Sb](F)F GUNJVIDCYZYFGV-UHFFFAOYSA-K 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- OYLGJCQECKOTOL-UHFFFAOYSA-L barium fluoride Chemical compound [F-].[F-].[Ba+2] OYLGJCQECKOTOL-UHFFFAOYSA-L 0.000 description 1
- 229910001632 barium fluoride Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 125000006575 electron-withdrawing group Chemical group 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000010813 internal standard method Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 235000019515 salmon Nutrition 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 235000013024 sodium fluoride Nutrition 0.000 description 1
- 239000011775 sodium fluoride Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910021561 transition metal fluoride Inorganic materials 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58024848A JPS59152361A (ja) | 1983-02-18 | 1983-02-18 | ペンタフルオロベンゾニトリルの製法 |
| EP84300911A EP0120575B1 (en) | 1983-02-18 | 1984-02-14 | Organic fluorine compounds |
| DE8484300911T DE3478681D1 (en) | 1983-02-18 | 1984-02-14 | Organic fluorine compounds |
| US06/776,085 US4684734A (en) | 1983-02-18 | 1985-09-13 | Method for manufacture or organic fluorine compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58024848A JPS59152361A (ja) | 1983-02-18 | 1983-02-18 | ペンタフルオロベンゾニトリルの製法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59152361A JPS59152361A (ja) | 1984-08-31 |
| JPS6224417B2 true JPS6224417B2 (en, 2012) | 1987-05-28 |
Family
ID=12149631
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58024848A Granted JPS59152361A (ja) | 1983-02-18 | 1983-02-18 | ペンタフルオロベンゾニトリルの製法 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59152361A (en, 2012) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6094919A (ja) * | 1983-10-31 | 1985-05-28 | Nippon Shokubai Kagaku Kogyo Co Ltd | 有機フツ素化物の製法 |
-
1983
- 1983-02-18 JP JP58024848A patent/JPS59152361A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59152361A (ja) | 1984-08-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4684734A (en) | Method for manufacture or organic fluorine compounds | |
| JPS6224417B2 (en, 2012) | ||
| JP6498048B2 (ja) | 含フッ素有機化合物及びこれとグリニャール試薬によるビアリール化合物の製造方法 | |
| JPH024580B2 (en, 2012) | ||
| JPS5824430B2 (ja) | フルオルベンゾニトリル類の製造方法 | |
| JP3452086B2 (ja) | パーフルオロアルコキシ（アルキルチオ）ベンゼン類の製造方法 | |
| JPH0313206B2 (en, 2012) | ||
| JP2736801B2 (ja) | ハロゲン化芳香族化合物のフッ素化方法 | |
| JP2005530793A (ja) | アルコキシベンゾニトリルの触媒不含の製造方法 | |
| JPH0258255B2 (en, 2012) | ||
| JPS6049170B2 (ja) | β−アルコキシエトキシメチルハライドの製造方法 | |
| US5336818A (en) | Process for the preparation of substantially fluorinated alkyl bromides | |
| JPS6132309B2 (en, 2012) | ||
| JPH0149337B2 (en, 2012) | ||
| JPS635023B2 (en, 2012) | ||
| JPS6147426A (ja) | フツ素化環式炭化水素類の製法 | |
| JP2662462B2 (ja) | ビアリールの製造方法 | |
| JPS6072851A (ja) | フツ化ベンゾニトリル類の製造方法 | |
| JPS6240353B2 (en, 2012) | ||
| JPS6153345B2 (en, 2012) | ||
| JPS627185B2 (en, 2012) | ||
| JPS6365058B2 (en, 2012) | ||
| JPH044309B2 (en, 2012) | ||
| JPS59155340A (ja) | 弗素化ニトロアルカンの製法 | |
| WO2021039230A1 (ja) | ｍ－ジアルキルベンズアルデヒドの製造方法 |