SU410026A1 - - Google Patents

Info

Publication number

SU410026A1

SU410026A1 SU1775983A SU1775983A SU410026A1 SU 410026 A1 SU410026 A1 SU 410026A1 SU 1775983 A SU1775983 A SU 1775983A SU 1775983 A SU1775983 A SU 1775983A SU 410026 A1 SU410026 A1 SU 410026A1

Authority

SU

USSR - Soviet Union

Prior art keywords

preparation

acids

mol

xanthogeno

dithiocarbaminoacetic

Prior art date

1972-04-21

Links

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• Global Dossier
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• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
• 238000000034 method Methods 0.000 description 9
• 239000002253 acid Substances 0.000 description 8
• 150000001875 compounds Chemical class 0.000 description 7
• 238000002360 preparation method Methods 0.000 description 7
• NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 6
• 150000007513 acids Chemical class 0.000 description 6
• 150000008064 anhydrides Chemical class 0.000 description 4
• 239000000047 product Substances 0.000 description 4
• QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
• 125000003545 alkoxy group Chemical group 0.000 description 3
• 125000003282 alkyl amino group Chemical group 0.000 description 3
• 238000006243 chemical reaction Methods 0.000 description 3
• 125000004663 dialkyl amino group Chemical group 0.000 description 3
• 150000003014 phosphoric acid esters Chemical class 0.000 description 3
• 238000003756 stirring Methods 0.000 description 3
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
• 125000000217 alkyl group Chemical group 0.000 description 2
• LGTLXDJOAJDFLR-UHFFFAOYSA-N diethyl chlorophosphate Chemical compound CCOP(Cl)(=O)OCC LGTLXDJOAJDFLR-UHFFFAOYSA-N 0.000 description 2
• ZJXZSIYSNXKHEA-UHFFFAOYSA-N ethyl dihydrogen phosphate Chemical compound CCOP(O)(O)=O ZJXZSIYSNXKHEA-UHFFFAOYSA-N 0.000 description 2
• 238000001914 filtration Methods 0.000 description 2
• 238000002329 infrared spectrum Methods 0.000 description 2
• 239000003960 organic solvent Substances 0.000 description 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
• OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
• 238000010521 absorption reaction Methods 0.000 description 1
• 239000013543 active substance Substances 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• 150000001735 carboxylic acids Chemical class 0.000 description 1
• 150000001805 chlorine compounds Chemical class 0.000 description 1
• FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
• 229940106681 chloroacetic acid Drugs 0.000 description 1
• 150000002148 esters Chemical class 0.000 description 1
• 239000000706 filtrate Substances 0.000 description 1
• 230000003993 interaction Effects 0.000 description 1
• 239000000543 intermediate Substances 0.000 description 1
• 238000002955 isolation Methods 0.000 description 1
• 239000007788 liquid Substances 0.000 description 1
• 229910052698 phosphorus Inorganic materials 0.000 description 1
• 239000011574 phosphorus Substances 0.000 description 1
• 239000002243 precursor Substances 0.000 description 1
• 150000003839 salts Chemical class 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 150000003512 tertiary amines Chemical class 0.000 description 1
• ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1