SU164597A1 - - Google Patents
Info
- Publication number
- SU164597A1 SU164597A1 SU860273A SU860273A SU164597A1 SU 164597 A1 SU164597 A1 SU 164597A1 SU 860273 A SU860273 A SU 860273A SU 860273 A SU860273 A SU 860273A SU 164597 A1 SU164597 A1 SU 164597A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- anisidine
- product
- acetamino
- methoxy
- acetyl
- Prior art date
Links
- NROKBHXJSPEDAR-UHFFFAOYSA-M potassium fluoride Chemical compound [F-].[K+] NROKBHXJSPEDAR-UHFFFAOYSA-M 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- FGOFNVXHDGQVBG-UHFFFAOYSA-N N-(2-methoxyphenyl)acetamide Chemical compound COC1=CC=CC=C1NC(C)=O FGOFNVXHDGQVBG-UHFFFAOYSA-N 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 description 3
- UQSQSQZYBQSBJZ-UHFFFAOYSA-N fluorosulfonic acid Chemical compound OS(F)(=O)=O UQSQSQZYBQSBJZ-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 235000003270 potassium fluoride Nutrition 0.000 description 3
- 239000011698 potassium fluoride Substances 0.000 description 3
- 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 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- PMSUSRFIJGPMJE-UHFFFAOYSA-N 3-acetamido-4-methoxybenzenesulfonic acid Chemical compound COC1=CC=C(S(O)(=O)=O)C=C1NC(C)=O PMSUSRFIJGPMJE-UHFFFAOYSA-N 0.000 description 1
- KRKMAUKQDRAOFI-UHFFFAOYSA-N 3-acetamido-4-methoxybenzenesulfonyl chloride Chemical compound COC1=CC=C(S(Cl)(=O)=O)C=C1NC(C)=O KRKMAUKQDRAOFI-UHFFFAOYSA-N 0.000 description 1
- DPQQVRWSRIMQLT-UHFFFAOYSA-N 3-acetamido-4-methoxybenzenesulfonyl fluoride Chemical compound COC1=CC=C(S(F)(=O)=O)C=C1NC(C)=O DPQQVRWSRIMQLT-UHFFFAOYSA-N 0.000 description 1
- -1 3-amino-4-methoxy-O-anisidine Chemical compound 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 230000021736 acetylation Effects 0.000 description 1
- 238000006640 acetylation reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- UNDANMCANJZUAA-UHFFFAOYSA-N benzene sulfurofluoridic acid Chemical compound S(=O)(=O)(O)F.C1=CC=CC=C1 UNDANMCANJZUAA-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU860273A SU164597A1 (https=) | 1963-10-08 | 1963-10-08 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SU860273A SU164597A1 (https=) | 1963-10-08 | 1963-10-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU164597A1 true SU164597A1 (https=) | 1964-08-19 |
Family
ID=40344738
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU860273A SU164597A1 (https=) | 1963-10-08 | 1963-10-08 |
Country Status (1)
| Country | Link |
|---|---|
| SU (1) | SU164597A1 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2484085C2 (ru) * | 2007-03-06 | 2013-06-10 | Зика Текнолоджи Аг | Диальдимин, эмульсия, содержащая диальдимин, а также двухкомпонентная полиуретановая композиция и ее применение |
| CN103524382A (zh) * | 2007-03-06 | 2014-01-22 | Sika技术股份公司 | 二醛亚胺、含有二醛亚胺的乳液，以及双组分聚氨酯组合物及其应用 |
-
1963
- 1963-10-08 SU SU860273A patent/SU164597A1/ru active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2484085C2 (ru) * | 2007-03-06 | 2013-06-10 | Зика Текнолоджи Аг | Диальдимин, эмульсия, содержащая диальдимин, а также двухкомпонентная полиуретановая композиция и ее применение |
| CN103524382A (zh) * | 2007-03-06 | 2014-01-22 | Sika技术股份公司 | 二醛亚胺、含有二醛亚胺的乳液，以及双组分聚氨酯组合物及其应用 |
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