JP4283990B2 - 高割合で１，５−ジニトロナフタレンを含有するジニトロナフタレンの異性体混合物の製造方法 - Google Patents
高割合で１，５−ジニトロナフタレンを含有するジニトロナフタレンの異性体混合物の製造方法 Download PDFInfo
- Publication number
- JP4283990B2 JP4283990B2 JP2000510700A JP2000510700A JP4283990B2 JP 4283990 B2 JP4283990 B2 JP 4283990B2 JP 2000510700 A JP2000510700 A JP 2000510700A JP 2000510700 A JP2000510700 A JP 2000510700A JP 4283990 B2 JP4283990 B2 JP 4283990B2
- Authority
- JP
- Japan
- Prior art keywords
- dinitronaphthalene
- nitration
- nitronaphthalene
- nitric acid
- weight
- 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 - Fee Related
Links
- 239000000203 mixture Substances 0.000 title claims description 33
- 238000000034 method Methods 0.000 title claims description 17
- XNKFCDGEFCOQOM-UHFFFAOYSA-N 1,2-dinitronaphthalene Chemical compound C1=CC=CC2=C([N+]([O-])=O)C([N+](=O)[O-])=CC=C21 XNKFCDGEFCOQOM-UHFFFAOYSA-N 0.000 title claims description 13
- ZUTCJXFCHHDFJS-UHFFFAOYSA-N 1,5-dinitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1[N+]([O-])=O ZUTCJXFCHHDFJS-UHFFFAOYSA-N 0.000 title claims description 10
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 35
- 229910017604 nitric acid Inorganic materials 0.000 claims description 35
- 238000006396 nitration reaction Methods 0.000 claims description 34
- RJKGJBPXVHTNJL-UHFFFAOYSA-N 1-nitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=CC2=C1 RJKGJBPXVHTNJL-UHFFFAOYSA-N 0.000 claims description 31
- 239000003960 organic solvent Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- 150000002500 ions Chemical class 0.000 claims description 7
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- AVCSMMMOCOTIHF-UHFFFAOYSA-N 1,8-dinitronaphthalene Chemical compound C1=CC([N+]([O-])=O)=C2C([N+](=O)[O-])=CC=CC2=C1 AVCSMMMOCOTIHF-UHFFFAOYSA-N 0.000 claims description 5
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical class O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000004971 nitroalkyl group Chemical group 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 19
- 238000006243 chemical reaction Methods 0.000 description 14
- 229920000557 Nafion® Polymers 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 150000007513 acids Chemical class 0.000 description 5
- 238000005259 measurement Methods 0.000 description 5
- 230000000802 nitrating effect Effects 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- SBJCUZQNHOLYMD-UHFFFAOYSA-N 1,5-Naphthalene diisocyanate Chemical compound C1=CC=C2C(N=C=O)=CC=CC2=C1N=C=O SBJCUZQNHOLYMD-UHFFFAOYSA-N 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- 239000011343 solid material Substances 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000004817 gas chromatography Methods 0.000 description 3
- 239000005457 ice water Substances 0.000 description 3
- LYGJENNIWJXYER-UHFFFAOYSA-N nitromethane Chemical compound C[N+]([O-])=O LYGJENNIWJXYER-UHFFFAOYSA-N 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- CUARLQDWYSRQDF-UHFFFAOYSA-N 5-Nitroacenaphthene Chemical compound C1CC2=CC=CC3=C2C1=CC=C3[N+](=O)[O-] CUARLQDWYSRQDF-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003930 superacid Substances 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- JCMBWDZBURXGMC-UHFFFAOYSA-N 1,3,6-trinitronaphthalene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC2=CC([N+](=O)[O-])=CC=C21 JCMBWDZBURXGMC-UHFFFAOYSA-N 0.000 description 1
- ZJYJZEAJZXVAMF-UHFFFAOYSA-N 2-nitronaphthalene Chemical compound C1=CC=CC2=CC([N+](=O)[O-])=CC=C21 ZJYJZEAJZXVAMF-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- XTVVROIMIGLXTD-UHFFFAOYSA-N copper(II) nitrate Chemical compound [Cu+2].[O-][N+]([O-])=O.[O-][N+]([O-])=O XTVVROIMIGLXTD-UHFFFAOYSA-N 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- KQSABULTKYLFEV-UHFFFAOYSA-N naphthalene-1,5-diamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1N KQSABULTKYLFEV-UHFFFAOYSA-N 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011949 solid catalyst Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/08—Preparation of nitro compounds by substitution of hydrogen atoms by nitro groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19739202.4 | 1997-09-08 | ||
| DE19739202A DE19739202C1 (de) | 1997-09-08 | 1997-09-08 | Verfahren zur Herstellung eines Dinitronaphthalin-Isomerengemisches mit hohem Anteil an 1,5-Dinitronaphthalin |
| PCT/EP1998/005408 WO1999012887A1 (de) | 1997-09-08 | 1998-08-26 | Verfahren zur herstellung eines dinitronaphthalin-isomerengemisches mit hohem anteil an 1,5-dinitronaphthalin |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001515878A JP2001515878A (ja) | 2001-09-25 |
| JP2001515878A5 JP2001515878A5 (https=) | 2006-01-05 |
| JP4283990B2 true JP4283990B2 (ja) | 2009-06-24 |
Family
ID=7841533
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000510700A Expired - Fee Related JP4283990B2 (ja) | 1997-09-08 | 1998-08-26 | 高割合で１，５−ジニトロナフタレンを含有するジニトロナフタレンの異性体混合物の製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6242656B1 (https=) |
| EP (1) | EP1015414B1 (https=) |
| JP (1) | JP4283990B2 (https=) |
| AU (1) | AU9347098A (https=) |
| DE (2) | DE19739202C1 (https=) |
| ES (1) | ES2241165T3 (https=) |
| WO (1) | WO1999012887A1 (https=) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19958389A1 (de) * | 1999-12-03 | 2001-06-07 | Bayer Ag | Verfahren zur Herstellung eines Dinitronaphthalin-Isomerengemisches mit erhöhtem Anteil an 1,5-Dinitronaphthalin |
| DE60230097D1 (de) | 2001-05-08 | 2009-01-15 | Mitsui Chemicals Polyurethanes | Verfahren zur herstellung von 1,5-diaminonaphthalinen |
| DE10209644A1 (de) * | 2002-03-05 | 2003-09-18 | Bayer Ag | Verfahren zur Herstellung eines Dinitronaphthalin-Isomerengemisches mit hohem Anteil an 1,5-Dinitronaphthalin |
| ATE520645T1 (de) * | 2003-11-05 | 2011-09-15 | Bayer Materialscience Ag | Verfahren zur herstellung von 1,5- dinitronaphthalen |
| JP2009062342A (ja) * | 2007-09-08 | 2009-03-26 | National Institute Of Advanced Industrial & Technology | 固体有機化合物のニトロ化溶媒の選定方法及び基質有機化合物のニトロ化反応方法 |
| CN102276475A (zh) * | 2011-06-24 | 2011-12-14 | 彭新华 | 一种合成1,5-二硝基萘和1,8-二硝基萘的方法 |
| CN102827006A (zh) * | 2012-09-20 | 2012-12-19 | 台州职业技术学院 | 一种利用固定床反应器催化硝化芳香族化合物的制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL103911C (https=) * | 1958-02-11 | |||
| DE1150965B (de) | 1961-09-22 | 1963-07-04 | Basf Ag | Verfahren zur kontinuierlichen Herstellung von 1, 5- und 1, 8-Dinitronaphthalin |
| DE2453529A1 (de) | 1974-11-12 | 1976-05-13 | Bayer Ag | Verfahren zur herstellung von nitronaphthalinen |
| US3976704A (en) * | 1975-01-06 | 1976-08-24 | Varen Technology | Nitration process |
| DE2517437C3 (de) * | 1975-04-19 | 1978-11-09 | Bayer Ag, 5090 Leverkusen | Verfahren zur Gewinnung von 13 - und 1,8 Dinitronaphthalin |
| PT101207A (pt) | 1993-02-26 | 1994-08-31 | Inst Nac De Engenharia E Tecno | Processo para a nitracao de compostos aromaticos em condicoes suaves e nao corrosivas |
-
1997
- 1997-09-08 DE DE19739202A patent/DE19739202C1/de not_active Expired - Lifetime
-
1998
- 1998-08-26 WO PCT/EP1998/005408 patent/WO1999012887A1/de not_active Ceased
- 1998-08-26 JP JP2000510700A patent/JP4283990B2/ja not_active Expired - Fee Related
- 1998-08-26 DE DE59812746T patent/DE59812746D1/de not_active Expired - Lifetime
- 1998-08-26 AU AU93470/98A patent/AU9347098A/en not_active Abandoned
- 1998-08-26 US US09/486,686 patent/US6242656B1/en not_active Expired - Lifetime
- 1998-08-26 EP EP98946431A patent/EP1015414B1/de not_active Expired - Lifetime
- 1998-08-26 ES ES98946431T patent/ES2241165T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE19739202C1 (de) | 1999-03-25 |
| AU9347098A (en) | 1999-03-29 |
| EP1015414B1 (de) | 2005-04-20 |
| WO1999012887A1 (de) | 1999-03-18 |
| ES2241165T3 (es) | 2005-10-16 |
| US6242656B1 (en) | 2001-06-05 |
| JP2001515878A (ja) | 2001-09-25 |
| EP1015414A1 (de) | 2000-07-05 |
| DE59812746D1 (de) | 2005-05-25 |
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