JPS60116639A - モノ‐またはジ‐クロルフエノール類の異性化法 - Google Patents
モノ‐またはジ‐クロルフエノール類の異性化法Info
- Publication number
- JPS60116639A JPS60116639A JP23534184A JP23534184A JPS60116639A JP S60116639 A JPS60116639 A JP S60116639A JP 23534184 A JP23534184 A JP 23534184A JP 23534184 A JP23534184 A JP 23534184A JP S60116639 A JPS60116639 A JP S60116639A
- Authority
- JP
- Japan
- Prior art keywords
- dichlorophenol
- chlorophenol
- zeolite
- reactor
- type
- 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.)
- Granted
Links
- UMPSXRYVXUPCOS-UHFFFAOYSA-N 2,3-dichlorophenol Chemical class OC1=CC=CC(Cl)=C1Cl UMPSXRYVXUPCOS-UHFFFAOYSA-N 0.000 title claims description 21
- 238000006317 isomerization reaction Methods 0.000 title description 9
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims description 26
- 239000010457 zeolite Substances 0.000 claims description 26
- 229910021536 Zeolite Inorganic materials 0.000 claims description 22
- 239000003054 catalyst Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 18
- WXNZTHHGJRFXKQ-UHFFFAOYSA-N 4-chlorophenol Chemical class OC1=CC=C(Cl)C=C1 WXNZTHHGJRFXKQ-UHFFFAOYSA-N 0.000 claims description 15
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- HFZWRUODUSTPEG-UHFFFAOYSA-N 2,4-dichlorophenol Chemical compound OC1=CC=C(Cl)C=C1Cl HFZWRUODUSTPEG-UHFFFAOYSA-N 0.000 claims description 5
- RANCECPPZPIPNO-UHFFFAOYSA-N 2,5-dichlorophenol Chemical compound OC1=CC(Cl)=CC=C1Cl RANCECPPZPIPNO-UHFFFAOYSA-N 0.000 claims description 4
- HORNXRXVQWOLPJ-UHFFFAOYSA-N 3-chlorophenol Chemical compound OC1=CC=CC(Cl)=C1 HORNXRXVQWOLPJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052680 mordenite Inorganic materials 0.000 claims description 3
- 239000012013 faujasite Substances 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims 2
- 150000001768 cations Chemical class 0.000 claims 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 8
- 238000001704 evaporation Methods 0.000 description 8
- 230000008020 evaporation Effects 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 239000007789 gas Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- 239000007858 starting material Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000005660 chlorination reaction Methods 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000012159 carrier gas Substances 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 238000001354 calcination Methods 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- 150000001340 alkali metals Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000006193 diazotization reaction Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000007040 multi-step synthesis reaction Methods 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical class ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- VGVRPFIJEJYOFN-UHFFFAOYSA-N 2,3,4,6-tetrachlorophenol Chemical class OC1=C(Cl)C=C(Cl)C(Cl)=C1Cl VGVRPFIJEJYOFN-UHFFFAOYSA-N 0.000 description 1
- WDNBURPWRNALGP-UHFFFAOYSA-N 3,4-Dichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1 WDNBURPWRNALGP-UHFFFAOYSA-N 0.000 description 1
- PNPCRKVUWYDDST-UHFFFAOYSA-N 3-chloroaniline Chemical compound NC1=CC=CC(Cl)=C1 PNPCRKVUWYDDST-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 229910001420 alkaline earth metal ion Inorganic materials 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 150000002366 halogen compounds Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004811 liquid chromatography Methods 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229910052756 noble gas Inorganic materials 0.000 description 1
- 150000002835 noble gases Chemical class 0.000 description 1
- 238000011017 operating method Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229910052615 phyllosilicate Inorganic materials 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- -1 rare earth metal ions Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19833340997 DE3340997A1 (de) | 1983-11-12 | 1983-11-12 | Verfahren zur isomerisierung von chlorphenolen |
DE3340997.8 | 1983-11-12 | ||
DE3345808.1 | 1983-12-17 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS60116639A true JPS60116639A (ja) | 1985-06-24 |
JPH0453854B2 JPH0453854B2 (enrdf_load_stackoverflow) | 1992-08-27 |
Family
ID=6214176
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP23534184A Granted JPS60116639A (ja) | 1983-11-12 | 1984-11-09 | モノ‐またはジ‐クロルフエノール類の異性化法 |
Country Status (2)
Country | Link |
---|---|
JP (1) | JPS60116639A (enrdf_load_stackoverflow) |
DE (1) | DE3340997A1 (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017530150A (ja) * | 2014-10-02 | 2017-10-12 | モンサント テクノロジー エルエルシー | 2,5−ジクロロフェノールの合成方法 |
-
1983
- 1983-11-12 DE DE19833340997 patent/DE3340997A1/de not_active Withdrawn
-
1984
- 1984-11-09 JP JP23534184A patent/JPS60116639A/ja active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2017530150A (ja) * | 2014-10-02 | 2017-10-12 | モンサント テクノロジー エルエルシー | 2,5−ジクロロフェノールの合成方法 |
Also Published As
Publication number | Publication date |
---|---|
JPH0453854B2 (enrdf_load_stackoverflow) | 1992-08-27 |
DE3340997A1 (de) | 1985-05-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5137854A (en) | Process for the production of modified H-mordenite, catalyst comprising said H-mordenite and process for the synthesis of methylamine with the use of the same | |
JPS59206323A (ja) | フエノ−ル及びアセトンの製造方法 | |
EP0118851B1 (en) | Process for producing a chlorohalobenzene | |
JPS63201135A (ja) | 2,6−ジアルキルナフタリンの製造法 | |
JP2583483B2 (ja) | ハロゲン化ベンゼン誘導体の製造法 | |
US4935561A (en) | Process for isomerizing monochlorotoluenes or dichlorotoluenes | |
US4568777A (en) | Process for isomerizing monochlorophenols or dichlorophenols | |
US4426543A (en) | Vapor phase nitration of aromatic hydrocarbons | |
JPS60116639A (ja) | モノ‐またはジ‐クロルフエノール類の異性化法 | |
JP4695069B2 (ja) | 6−クロロ−2−トリクロロメチルピリジンの気相塩素化による3,6−ジクロロ−2−トリクロロメチルピリジンの製造 | |
US4604470A (en) | Process for the isomerization of halogenated thiophenes | |
JPH0278640A (ja) | チモールの製造方法 | |
CA2049908A1 (en) | Process for the preparation of acylbenzenes | |
CA1275115A (en) | Process for producing a halogenated benzene derivative using an improved zeolite catalyst | |
US5210308A (en) | Process for the production of modified H-mordenite, catalyst comprising said H-mordenite and process for the synthesis of methylamine with the use of the same | |
US5002639A (en) | Separation of ortho-, meta- and para-tolunitrile from ternary mixtures of the isomers | |
JPS611629A (ja) | モノ‐又はジクロルトエンの異性化法 | |
JPS61112040A (ja) | フエニルアセトアルデヒド類の製造方法 | |
JPH04275241A (ja) | 3,3’,4,4’−テトラメチルジフェニルメタンの製造方法 | |
JPH03170442A (ja) | ベンジルビフェニルの製造方法 | |
JPS6372640A (ja) | ジフエニルエ−テル類の製造方法 | |
Dagade | Nitration of aromatic compounds over solid acid catalysts | |
JP2595650B2 (ja) | パラ置換塩素化ベンゼン誘導体の高選択的製造法 | |
DE3345808A1 (de) | Verfahren zur isomerisierung von dichlorphenolen | |
GB2090281A (en) | Para-selective Methylation of Ethylbenzene |