BE635013A - - Google Patents
Info
- Publication number
- BE635013A BE635013A BE635013DA BE635013A BE 635013 A BE635013 A BE 635013A BE 635013D A BE635013D A BE 635013DA BE 635013 A BE635013 A BE 635013A
- Authority
- BE
- Belgium
- Prior art keywords
- emi
- parts
- sodium
- compounds
- reaction
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000001174 sulfone group Chemical group 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- GRWZHXKQBITJKP-UHFFFAOYSA-L dithionite(2-) Chemical compound [O-]S(=O)S([O-])=O GRWZHXKQBITJKP-UHFFFAOYSA-L 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 2
- ZQHJVIHCDHJVII-OWOJBTEDSA-N (e)-2-chlorobut-2-enedioic acid Chemical class OC(=O)\C=C(\Cl)C(O)=O ZQHJVIHCDHJVII-OWOJBTEDSA-N 0.000 description 1
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- SQBJBZVNGGZASY-UHFFFAOYSA-N [Na].ClS(=O)(=O)O Chemical compound [Na].ClS(=O)(=O)O SQBJBZVNGGZASY-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- -1 alkyl vinyl sulfides Chemical class 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 125000004969 haloethyl group Chemical group 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- PFXVKGGZWQQTSE-UHFFFAOYSA-N sulfuryl dicyanide Chemical compound N#CS(=O)(=O)C#N PFXVKGGZWQQTSE-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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR941592A FR1363046A (fr) | 1963-07-16 | 1963-07-16 | Procédé de production de vinylsulfones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE635013A true BE635013A (d) |
Family
ID=8808403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE635013D BE635013A (d) | 1963-07-16 |
Country Status (2)
| Country | Link |
|---|---|
| BE (1) | BE635013A (d) |
| FR (1) | FR1363046A (d) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR3015433B1 (fr) | 2013-12-23 | 2016-02-12 | Airbus Operations Sas | Ensemble pour aeronef comprenant un mat d'accrochage integre a la nacelle et agence en partie arriere du fuselage |
| CN105732446B (zh) * | 2016-02-05 | 2017-05-24 | 上海优合生物科技有限公司 | 一种双（乙烯基砜）甲烷的中间体双（2‑氯乙基砜基）甲烷的制备方法 |
-
0
- BE BE635013D patent/BE635013A/fr unknown
-
1963
- 1963-07-16 FR FR941592A patent/FR1363046A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR1363046A (fr) | 1964-06-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA1290764C (en) | Preparation of sulphonated aromatic esters | |
| EP0237446B1 (fr) | Procédé de préparation d'acides perhalogénométhanesulfiniques et sulfoniques et de leurs sels | |
| BE635013A (d) | ||
| US2999879A (en) | Process for the production of aromatic carboxylic acids | |
| SU1594169A1 (ru) | Способ получени 5-бромпентановой кислоты | |
| EP1208076B1 (en) | Process for the preparation of alkanoyloxy-benzenesulfonic acids and salts thereof | |
| FR2583040A1 (fr) | Procede pour la production de 2,6-naphtalenediol et de 2,6-diacetoxynaphtalene | |
| FR2508041A1 (fr) | Procede de production d'ester nicotinylique de l'acide 6-aminonicotinique | |
| US3536746A (en) | Preparation of 7-chloro-4-thiaoenanthic acid | |
| CH615921A5 (en) | Process for the preparation of 1-carbamoyl-3-(3,5-dichlorophenyl)hydantoins | |
| FR2614298A1 (fr) | Procede de preparation de l'acide trifluoromethylbenzoique a partir d'hexafluoroxylene. | |
| FR2705669A1 (fr) | Procédé de préparation d'acides hydroxyphénylacétiques. | |
| BE1005616A4 (fr) | Procede de purification du sulfate d'ammonium. | |
| JPS599533B2 (ja) | ジオキシジフエニルの製造法 | |
| FR2572398A1 (fr) | Procede a une etape pour preparer un bis-(amino-nitro-phenyl)-methane | |
| KR100278967B1 (ko) | 오르쏘-디플루오로벤조산 유도체의 제조방법 | |
| CH220046A (fr) | Procédé de préparation d'un dérivé de la para-amino-benzène-sulfamide. | |
| CH222734A (fr) | Procédé de préparation d'un dérivé de la para-amino-benzène-sulfamide. | |
| FR2507599A1 (fr) | Procede de preparation de derives de sulfimide d'acide n-carbamoylbenzoique | |
| JPS58150561A (ja) | スルホニルハイドロキノン類の製法 | |
| CH401957A (fr) | Procédé perfectionné de préparation d'esters tricycliques non saturés | |
| EP0151835A1 (en) | Process for producing pentachloronitrobenzene from hexachlorobenzene | |
| CH222733A (fr) | Procédé de préparation d'un dérivé de la para-amino-benzène-sulfamide. | |
| BE563583A (d) | ||
| CH271931A (fr) | Procédé de préparation du bromure de 2-bromo-2-formyl-éthyl-pyridinium. |