JP2010510258A5 - - Google Patents

Info

Publication number

JP2010510258A5

JP2010510258A5 JP2009537502A JP2009537502A JP2010510258A5 JP 2010510258 A5 JP2010510258 A5 JP 2010510258A5 JP 2009537502 A JP2009537502 A JP 2009537502A JP 2009537502 A JP2009537502 A JP 2009537502A JP 2010510258 A5 JP2010510258 A5 JP 2010510258A5

Authority

JP

Japan

Prior art keywords

butyl

tert

methyl

isobutyl

ketoxime

Prior art date

2007-11-03

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.)

Abandoned

Links

• Espacenet
• Global Dossier
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• 238000000034 method Methods 0.000 claims 20
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 16
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 16
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 11
• PNLIHZUUWJIBEP-UHFFFAOYSA-N 3-hydroxyiminopentane-1,5-diol Chemical compound OCCC(=NO)CCO PNLIHZUUWJIBEP-UHFFFAOYSA-N 0.000 claims 8
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims 6
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 6
• 239000002253 acid Substances 0.000 claims 5
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 5
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 5
• WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 claims 4
• 229910052736 halogen Inorganic materials 0.000 claims 4
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 4
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 4
• UXFQFBNBSPQBJW-UHFFFAOYSA-N 2-amino-2-methylpropane-1,3-diol Chemical compound OCC(N)(C)CO UXFQFBNBSPQBJW-UHFFFAOYSA-N 0.000 claims 3
• IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 3
• 150000002367 halogens Chemical class 0.000 claims 3
• 239000007864 aqueous solution Substances 0.000 claims 2
• 125000005843 halogen group Chemical group 0.000 claims 2
• 150000007529 inorganic bases Chemical class 0.000 claims 2
• 125000000896 monocarboxylic acid group Chemical group 0.000 claims 2
• 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
• 150000007530 organic bases Chemical class 0.000 claims 2
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
• JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 2
• 125000000217 alkyl group Chemical group 0.000 claims 1
• 150000007522 mineralic acids Chemical class 0.000 claims 1
• 150000007524 organic acids Chemical class 0.000 claims 1