SU413144A1 - - Google Patents
Info
- Publication number
- SU413144A1 SU413144A1 SU1762565A SU1762565A SU413144A1 SU 413144 A1 SU413144 A1 SU 413144A1 SU 1762565 A SU1762565 A SU 1762565A SU 1762565 A SU1762565 A SU 1762565A SU 413144 A1 SU413144 A1 SU 413144A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- xylene
- sulfonic acid
- acid
- sulfuric acid
- yield
- Prior art date
Links
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 239000008096 xylene Substances 0.000 description 7
- CZZZABOKJQXEBO-UHFFFAOYSA-N 2,4-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1 CZZZABOKJQXEBO-UHFFFAOYSA-N 0.000 description 2
- TUAMRELNJMMDMT-UHFFFAOYSA-N 3,5-xylenol Chemical compound CC1=CC(C)=CC(O)=C1 TUAMRELNJMMDMT-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000006396 nitration reaction Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- TYFFMMDREMDCGM-UHFFFAOYSA-N (1,5-dimethylcyclohexa-2,4-dien-1-yl) dihydrogen phosphate Chemical compound C1(CC(=CC=C1)C)(C)OP(O)(O)=O TYFFMMDREMDCGM-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 240000006909 Tilia x europaea Species 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 239000003708 ampul Substances 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- 239000012897 dilution medium Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001030 gas--liquid chromatography Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000006317 isomerization reaction Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000006722 reduction reaction Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 125000001174 sulfone group Chemical group 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1762565A SU413144A1 (enrdf_load_stackoverflow) | 1972-03-22 | 1972-03-22 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU1762565A SU413144A1 (enrdf_load_stackoverflow) | 1972-03-22 | 1972-03-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
SU413144A1 true SU413144A1 (enrdf_load_stackoverflow) | 1974-01-30 |
Family
ID=20507517
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU1762565A SU413144A1 (enrdf_load_stackoverflow) | 1972-03-22 | 1972-03-22 |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU413144A1 (enrdf_load_stackoverflow) |
-
1972
- 1972-03-22 SU SU1762565A patent/SU413144A1/ru active
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3772379A (en) | Preparation of dialkali dihydroxybenzene disulfonates | |
SU413144A1 (enrdf_load_stackoverflow) | ||
JPS6338334B2 (enrdf_load_stackoverflow) | ||
US405938A (en) | Gesellschapt fur anilin fabrikation | |
US3979445A (en) | Process for producing amino G acid and amino J acid from tobias acid | |
SU888818A3 (ru) | Способ получени (2,2-диметил-1,2-дигидрохинолин-4-ил)-метилусульфокислоты или ее солей | |
SU445662A1 (ru) | Способ получени 4-амино-3,5,6трихлорпиколиновой кислоты | |
US2501831A (en) | Process to produce 2, 6 dichlor-4-nitroaniline | |
SU463317A1 (ru) | Способ получени бис- (1-хлор-2-оксопергидроби-фенилил-3) -метана | |
US2835708A (en) | Process for the manufacture of resorcinol | |
Crowell et al. | Some Derivatives of p-DICHLOROBENZENE. 2 | |
SU232259A1 (ru) | Способ получения n-арилсульфоксинафталоимидов | |
SU296768A1 (ru) | Способ получения натриевых солей моносульфокислот диметиланилина | |
SU426479A1 (ru) | Способ получения сультонов | |
US1842163A (en) | Diaryl ether derivative | |
SU569553A1 (ru) | Способ получени 1,3,5 -триформилбензола | |
SU296769A1 (ru) | ВСЕСОЮЗНАЯ jр •ТТ'.3'";-'1_'''' '^^'(^''Т'Чл-'-БИБЛИОТЕКА | |
SU184268A1 (ru) | Способ получения флуорантен-4-сульфокислоты | |
SU459467A1 (ru) | Способ получени оротовой или 2-тиооротовой кислоты | |
SU485103A1 (ru) | Способ получени орто-замещенных метилен-бис-и трис-алкилфенолов | |
SU459068A1 (ru) | Способ получени бензоамидооксиуксусных кислот | |
SU421687A1 (ru) | Способ получения 1-адамантанкарбоновойкислоты | |
SU369793A1 (enrdf_load_stackoverflow) | ||
SU316680A1 (ru) | Способ получения 1-бром-з-бромметиладамантана | |
SU165699A1 (enrdf_load_stackoverflow) |