ES250300A1 - Un metodo para la preparaciën de un compuesto de amonio cuaternario - Google Patents

Info

Publication number

ES250300A1

ES250300A1 ES0250300A ES250300A ES250300A1 ES 250300 A1 ES250300 A1 ES 250300A1 ES 0250300 A ES0250300 A ES 0250300A ES 250300 A ES250300 A ES 250300A ES 250300 A1 ES250300 A1 ES 250300A1

Authority

ES

Spain

Prior art keywords

group

halogen atoms

groups

hydrogen

ethyl

Prior art date

1958-07-01

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Expired

Links

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• 238000000034 method Methods 0.000 title abstract 2
• 150000001875 compounds Chemical class 0.000 title 1
• 125000001453 quaternary ammonium group Chemical group 0.000 title 1
• 125000005843 halogen group Chemical group 0.000 abstract 5
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 4
• 229910052739 hydrogen Inorganic materials 0.000 abstract 4
• 239000001257 hydrogen Substances 0.000 abstract 4
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 4
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
• -1 isobutyryl Chemical group 0.000 abstract 3
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
• 125000003545 alkoxy group Chemical group 0.000 abstract 2
• 125000000217 alkyl group Chemical group 0.000 abstract 2
• 125000004432 carbon atom Chemical group C* 0.000 abstract 2
• 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
• 150000003856 quaternary ammonium compounds Chemical class 0.000 abstract 2
• 125000001424 substituent group Chemical group 0.000 abstract 2
• 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 abstract 1
• 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 abstract 1
• 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
• 125000004429 atom Chemical group 0.000 abstract 1
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
• 150000001768 cations Chemical class 0.000 abstract 1
• 238000006243 chemical reaction Methods 0.000 abstract 1
• 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 abstract 1
• 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
• 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 abstract 1
• 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 abstract 1
• 238000005956 quaternization reaction Methods 0.000 abstract 1
• 150000003512 tertiary amines Chemical class 0.000 abstract 1