BE453995A - - Google Patents
Info
- Publication number
- BE453995A BE453995A BE453995DA BE453995A BE 453995 A BE453995 A BE 453995A BE 453995D A BE453995D A BE 453995DA BE 453995 A BE453995 A BE 453995A
- Authority
- BE
- Belgium
- Prior art keywords
- parts
- vinyl
- weight
- sulfone
- aryl
- Prior art date
Links
- 238000006396 nitration reaction Methods 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 230000000875 corresponding Effects 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 125000003609 aryl vinyl group Chemical group 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N Carbon tetrachloride Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- FWFGVMYFCODZRD-UHFFFAOYSA-N oxidanium;hydrogen sulfate Chemical compound O.OS(O)(=O)=O FWFGVMYFCODZRD-UHFFFAOYSA-N 0.000 description 3
- YUYKFEBTTLESGR-UHFFFAOYSA-N [N+](=O)([O-])C(=CS(=O)(=O)C=C([N+](=O)[O-])C1=C(C=CC=C1)C)C1=C(C=CC=C1)C Chemical compound [N+](=O)([O-])C(=CS(=O)(=O)C=C([N+](=O)[O-])C1=C(C=CC=C1)C)C1=C(C=CC=C1)C YUYKFEBTTLESGR-UHFFFAOYSA-N 0.000 description 2
- CFUPZEDDCSQYNV-UHFFFAOYSA-N [N+](=O)([O-])C(=CS(=O)(=O)C=C([N+](=O)[O-])C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound [N+](=O)([O-])C(=CS(=O)(=O)C=C([N+](=O)[O-])C1=CC=CC=C1)C1=CC=CC=C1 CFUPZEDDCSQYNV-UHFFFAOYSA-N 0.000 description 2
- -1 aryl-vinyl sulfones Chemical class 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- UJTPZISIAWDGFF-UHFFFAOYSA-N ethenylsulfonylbenzene Chemical compound C=CS(=O)(=O)C1=CC=CC=C1 UJTPZISIAWDGFF-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- VKVLTUQLNXVANB-UHFFFAOYSA-N 1-ethenyl-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1C=C VKVLTUQLNXVANB-UHFFFAOYSA-N 0.000 description 1
- DRBHJBCQVUGCME-UHFFFAOYSA-N [N+](=O)([O-])C(=C(C1=CC=CC=C1)Cl)S(=O)(=O)C(=C(Cl)C1=CC=CC=C1)[N+](=O)[O-] Chemical compound [N+](=O)([O-])C(=C(C1=CC=CC=C1)Cl)S(=O)(=O)C(=C(Cl)C1=CC=CC=C1)[N+](=O)[O-] DRBHJBCQVUGCME-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005755 formation reaction Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001264 neutralization Effects 0.000 description 1
- HJHXMCYQJCTPCV-UHFFFAOYSA-N nitrosulfonylbenzene Chemical compound [O-][N+](=O)S(=O)(=O)C1=CC=CC=C1 HJHXMCYQJCTPCV-UHFFFAOYSA-N 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004753 textile 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
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/04—Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE453995A true BE453995A (ru) |
Family
ID=108246
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE453995D BE453995A (ru) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE453995A (ru) |
-
0
- BE BE453995D patent/BE453995A/fr unknown
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