BE694724A - - Google Patents
Info
- Publication number
- BE694724A BE694724A BE694724DA BE694724A BE 694724 A BE694724 A BE 694724A BE 694724D A BE694724D A BE 694724DA BE 694724 A BE694724 A BE 694724A
- Authority
- BE
- Belgium
- Prior art keywords
- acid
- nitrosyl
- anhydride
- sulfuric
- reacted
- Prior art date
Links
- 239000002253 acid Substances 0.000 claims description 30
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 19
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical group O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 claims description 18
- AKEJUJNQAAGONA-UHFFFAOYSA-N sulfur trioxide Chemical compound O=S(=O)=O AKEJUJNQAAGONA-UHFFFAOYSA-N 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 14
- LZDSILRDTDCIQT-UHFFFAOYSA-N dinitrogen trioxide Chemical compound [O-][N+](=O)N=O LZDSILRDTDCIQT-UHFFFAOYSA-N 0.000 claims description 10
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 9
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 6
- DSCYWCWECFREEJ-UHFFFAOYSA-N nitroso nitrosooxysulfonyl sulfate Chemical compound O=NOS(=O)(=O)OS(=O)(=O)ON=O DSCYWCWECFREEJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000004157 Nitrosyl chloride Substances 0.000 claims description 5
- VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 claims description 5
- 235000019392 nitrosyl chloride Nutrition 0.000 claims description 5
- LGKSIUWJPULKQS-UHFFFAOYSA-N chlorosulfonyl nitrite Chemical compound N(=O)OS(=O)(=O)Cl LGKSIUWJPULKQS-UHFFFAOYSA-N 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 5
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 5
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical class O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- -1 hydrochloride anhydride Chemical class 0.000 description 2
- HSSFHZJIMRUXDM-UHFFFAOYSA-N hydroxy(oxo)azanium chloride Chemical compound Cl.[O-][NH+]=O HSSFHZJIMRUXDM-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 206010015137 Eructation Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 101100349149 Schizosaccharomyces pombe (strain 972 / ATCC 24843) nse2 gene Proteins 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000003951 lactams Chemical class 0.000 description 1
- YNGRGHODNDCZCC-UHFFFAOYSA-N nitro hydrogen sulfate Chemical compound OS(=O)(=O)O[N+]([O-])=O YNGRGHODNDCZCC-UHFFFAOYSA-N 0.000 description 1
- VQTGUFBGYOIUFS-UHFFFAOYSA-N nitrosylsulfuric acid Chemical compound OS(=O)(=O)ON=O VQTGUFBGYOIUFS-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 239000001117 sulphuric acid Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B21/00—Nitrogen; Compounds thereof
- C01B21/082—Compounds containing nitrogen and non-metals and optionally metals
- C01B21/086—Compounds containing nitrogen and non-metals and optionally metals containing one or more sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT1498966 | 1966-02-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
BE694724A true BE694724A (enrdf_load_stackoverflow) | 1967-08-28 |
Family
ID=11146174
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BE694724D BE694724A (enrdf_load_stackoverflow) | 1966-02-28 | 1967-02-27 |
Country Status (6)
Country | Link |
---|---|
BE (1) | BE694724A (enrdf_load_stackoverflow) |
ES (1) | ES337943A1 (enrdf_load_stackoverflow) |
GR (1) | GR33357B (enrdf_load_stackoverflow) |
IL (1) | IL27482A (enrdf_load_stackoverflow) |
LU (1) | LU52931A1 (enrdf_load_stackoverflow) |
SE (1) | SE306726B (enrdf_load_stackoverflow) |
-
1967
- 1967-02-03 LU LU52931D patent/LU52931A1/xx unknown
- 1967-02-21 GR GR670133357A patent/GR33357B/el unknown
- 1967-02-24 IL IL2748267A patent/IL27482A/en unknown
- 1967-02-27 SE SE267167A patent/SE306726B/xx unknown
- 1967-02-27 ES ES337943A patent/ES337943A1/es not_active Expired
- 1967-02-27 BE BE694724D patent/BE694724A/fr unknown
Also Published As
Publication number | Publication date |
---|---|
ES337943A1 (es) | 1968-03-16 |
IL27482A (en) | 1970-05-21 |
SE306726B (enrdf_load_stackoverflow) | 1968-12-09 |
GR33357B (el) | 1967-11-28 |
LU52931A1 (enrdf_load_stackoverflow) | 1967-04-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP2006505597A (ja) | プソイドイオノンおよびイオノンの連続的製造方法 | |
JPH02169565A (ja) | ビス―(4―クロルフェニル)スルホンの製造方法 | |
BE694724A (enrdf_load_stackoverflow) | ||
US2102350A (en) | Process for manufacturing amino sulphonic acid | |
WO2001074754A1 (fr) | Procede de preparation de nitrites d'alkyles | |
US3227753A (en) | Manufacture of biurea | |
US4454362A (en) | Process for producing pentachloronitrobenzene | |
JPS5855452A (ja) | 1−ナフチルアミン−4,8−ジスルホン酸の製造方法 | |
US4461918A (en) | Process for producing pentachloronitrobenzene from hexachlorobenzene | |
JPS6144855B2 (enrdf_load_stackoverflow) | ||
US4225504A (en) | Monomeric N-methyleneaminoacetonitrile | |
US4341902A (en) | Process for the production of 5-nitro-acet-2,4-xylidine | |
JPS627910B2 (enrdf_load_stackoverflow) | ||
JPH0413657A (ja) | 2,4―ジアミノベンゼンスルホン酸の製造方法 | |
JPH04210954A (ja) | 1−アミノ−8−ヒドロキシナフタレン−3・6−ジスルホン酸の製造法 | |
US4943654A (en) | Process for preparation of α-acetoxy-α-methyl-N,N'-diacetyl malonamide | |
US6307033B1 (en) | Reactive blue dyes containing monochlorotriazine and acetoxyethyl sulfone groups | |
KR950002602B1 (ko) | 2-아미노 에틸 하이드로젼 설페이트의 제조방법 | |
KR910001437B1 (ko) | 1-아미노-2-브로모-4-히드록시 안트라퀴논의 제조방법 | |
BE635013A (enrdf_load_stackoverflow) | ||
BE453995A (enrdf_load_stackoverflow) | ||
BE721781A (enrdf_load_stackoverflow) | ||
HU187560B (en) | Process for production of sulphat of nickel | |
FR2616786A1 (fr) | Procede pour la preparation d'acides sulfoniques aliphatiques | |
Flowers et al. | Novel aspects in the reaction of 2-diazo-2′-(phenylthio) acetophenone with arenesulphenyl chlorides: formation of α-ketoaldehyde thioacetal chlorides via cyclic sulphonium α-(arylthio) phenacylides |