SU403164A1 - - Google Patents
Info
- Publication number
- SU403164A1 SU403164A1 SU1445800A SU1445800A SU403164A1 SU 403164 A1 SU403164 A1 SU 403164A1 SU 1445800 A SU1445800 A SU 1445800A SU 1445800 A SU1445800 A SU 1445800A SU 403164 A1 SU403164 A1 SU 403164A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- mol
- water
- product
- added
- phosphorus trichloride
- Prior art date
Links
- 239000000047 product Substances 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- FAIAAWCVCHQXDN-UHFFFAOYSA-N Phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 8
- 239000001257 hydrogen Substances 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 238000001953 recrystallisation Methods 0.000 description 7
- 229910052736 halogen Chemical group 0.000 description 6
- 150000002367 halogens Chemical group 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000012043 crude product Substances 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- FOCAUTSVDIKZOP-UHFFFAOYSA-N Chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 4
- 150000002431 hydrogen Chemical class 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 238000009835 boiling Methods 0.000 description 3
- 125000004432 carbon atoms Chemical group C* 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-Methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 2
- 150000001448 anilines Chemical class 0.000 description 2
- 229940106681 chloroacetic acid Drugs 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N 1-Hexanol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 1
- XHVCFGZWBIJJDZ-UHFFFAOYSA-N 2,2-dichloro-N-methyl-N-phenylacetamide Chemical compound ClC(Cl)C(=O)N(C)C1=CC=CC=C1 XHVCFGZWBIJJDZ-UHFFFAOYSA-N 0.000 description 1
- VUOFGWLJEBESHL-UHFFFAOYSA-N 2-chloro-N-methyl-N-phenylacetamide Chemical compound ClCC(=O)N(C)C1=CC=CC=C1 VUOFGWLJEBESHL-UHFFFAOYSA-N 0.000 description 1
- VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-N-phenylacetamide Chemical compound ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 1
- 229940051881 Anilide analgesics and antipyretics Drugs 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N Chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N Chloroformic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
- JXTHNDFMNIQAHM-UHFFFAOYSA-N Dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N Diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 229960004319 Trichloroacetic Acid Drugs 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N Trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229960005215 dichloroacetic acid Drugs 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HUNO000134 | 1969-06-07 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SU403164A1 true SU403164A1 (de) | |
| SU406381A1 SU406381A1 (de) | |
| SU403164A3 SU403164A3 (de) | 1973-10-19 |
Family
ID=11000020
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1445800A SU403164A3 (de) | 1969-06-07 | 1970-06-05 |
Country Status (12)
| Country | Link |
|---|---|
| AT (1) | AT303708B (de) |
| BE (1) | BE821883Q (de) |
| BG (1) | BG17536A3 (de) |
| CH (1) | CH535204A (de) |
| CS (1) | CS154302B2 (de) |
| DE (1) | DE2027822C3 (de) |
| FR (1) | FR2050066A5 (de) |
| GB (1) | GB1316782A (de) |
| PL (1) | PL82621B1 (de) |
| RO (1) | RO55298A (de) |
| SU (1) | SU403164A3 (de) |
| YU (1) | YU34664B (de) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4196142A (en) | 1977-03-04 | 1980-04-01 | American Cyanamid Company | 2-Chloro-n-isopropyl-3,5-disubstituted or 3,4,5-trisubstitutes lower alkyl acetanilides as herbicidal agents |
| DE4438001A1 (de) * | 1994-10-25 | 1996-05-02 | Bayer Ag | Herbizide Mittel auf Basis von N-(4-Fluor-phenyl)-N-isopropylchloracetamid und Verfahren zur Herstellung dieser Verbindung |
-
1970
- 1970-06-05 FR FR7020883A patent/FR2050066A5/fr not_active Expired
- 1970-06-05 DE DE19702027822 patent/DE2027822C3/de not_active Expired
- 1970-06-05 SU SU1445800A patent/SU403164A3/ru active
- 1970-06-05 CH CH850670A patent/CH535204A/de not_active IP Right Cessation
- 1970-06-05 CS CS397070A patent/CS154302B2/cs unknown
- 1970-06-05 YU YU144670A patent/YU34664B/xx unknown
- 1970-06-06 BG BG014883A patent/BG17536A3/xx unknown
- 1970-06-06 PL PL14113170A patent/PL82621B1/pl unknown
- 1970-06-08 RO RO6357970A patent/RO55298A/ro unknown
- 1970-06-08 GB GB2765270A patent/GB1316782A/en not_active Expired
- 1970-06-08 AT AT511270A patent/AT303708B/de not_active IP Right Cessation
-
1974
- 1974-11-05 BE BE150237A patent/BE821883Q/xx not_active IP Right Cessation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SU520041A3 (ru) | Способ получени амидов ароматических карбоновых кислот или их солей | |
| SU403164A1 (de) | ||
| US3539629A (en) | Process for producing tetraacetyl derivatives of diamines | |
| US4021442A (en) | Production of 1-alkyl-5-nitroimidazoles | |
| SU671723A3 (ru) | Способ получени пропан-1,2-диондиоксимов | |
| SU609464A3 (ru) | Способ получени производных -/2-пирролидинилметил/ бензамидов или их солей | |
| EP0124831B1 (de) | Verfahren zur Herstellung von O-Sulfonsäureestern gegebenenfalls substituierter Aminonaphthole | |
| EP0161617A2 (de) | Zwischenprodukte sowie Verfahren zur Herstellung von Zwischenproducten für die Synthese von Cephalosporinen | |
| US3960948A (en) | Substituted chloroacylanilides | |
| SU327682A1 (de) | ||
| US2820035A (en) | Barbituric acid derivatives | |
| SU242879A1 (ru) | Способ получения амидов | |
| SU416355A1 (de) | ||
| JPS6140222B2 (de) | ||
| SU170966A1 (ru) | Способ получения несимметричных диариламидов дитиомалоновой кислоты | |
| CH427839A (de) | Verfahren zur Herstellung von Sulfamylanthranilsäuren | |
| SU417941A3 (ru) | Способ получения замещенных тиоуреидобензола | |
| US2103558A (en) | Phosphates of amino acid esters and method of producing same | |
| SU327806A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ N,O-5/^C-AU,HJlXHHOH- ИМИНОКСИМОВ | |
| SU193516A1 (ru) | Способ получения |3- | |
| SU413679A3 (de) | ||
| SU340664A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ СМЕШАННЫХ АНГИДРИДОВсульФоновых и | |
| SU164596A1 (ru) | Способ получения хлорангидридов n-ароиларениминосульфокислот | |
| SU166684A1 (de) | ||
| SU237907A1 (ru) | Способ получения ;у-[5- |