SU365634A1 - - Google Patents

Info

Publication number

SU365634A1

SU365634A1 SU1425234A SU1425234A SU365634A1 SU 365634 A1 SU365634 A1 SU 365634A1 SU 1425234 A SU1425234 A SU 1425234A SU 1425234 A SU1425234 A SU 1425234A SU 365634 A1 SU365634 A1 SU 365634A1

Authority

SU

USSR - Soviet Union

Prior art keywords

laurinelactam

solution

carbon tetrachloride

nitrosyl chloride

equal

Prior art date

1970-04-07

Links

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• 239000004157 Nitrosyl chloride Substances 0.000 claims description 8
• VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 claims description 8
• 235000019392 nitrosyl chloride Nutrition 0.000 claims description 8
• 238000000034 method Methods 0.000 claims description 7
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
• 150000001875 compounds Chemical class 0.000 claims description 3
• 239000003960 organic solvent Substances 0.000 claims description 2
• 239000002904 solvent Substances 0.000 claims 2
• VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims 1
• VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 16
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
• 239000000203 mixture Substances 0.000 description 8
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
• 239000003513 alkali Substances 0.000 description 2
• 150000003951 lactams Chemical class 0.000 description 2
• 230000003287 optical effect Effects 0.000 description 2
• 239000000523 sample Substances 0.000 description 2
• ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 1
• 239000012491 analyte Substances 0.000 description 1
• 238000004821 distillation Methods 0.000 description 1
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
• -1 for example Substances 0.000 description 1
• 238000010438 heat treatment Methods 0.000 description 1
• 229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 1
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
• 239000012488 sample solution Substances 0.000 description 1
• 239000000126 substance Substances 0.000 description 1
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
• 238000005303 weighing Methods 0.000 description 1