JP2005518460A5 - - Google Patents

Info

Publication number

JP2005518460A5

JP2005518460A5 JP2003526976A JP2003526976A JP2005518460A5 JP 2005518460 A5 JP2005518460 A5 JP 2005518460A5 JP 2003526976 A JP2003526976 A JP 2003526976A JP 2003526976 A JP2003526976 A JP 2003526976A JP 2005518460 A5 JP2005518460 A5 JP 2005518460A5

Authority

JP

Japan

Prior art keywords

polycarbonate

group

bis

carbonate

phenyloxycarbonyl

Prior art date

2002-08-13

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.)

Granted

Links

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• -1 phenoxy, benzyl Chemical group 0.000 claims 18
• 229920000515 polycarbonate Polymers 0.000 claims 14
• 239000004417 polycarbonate Substances 0.000 claims 14
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 11
• 238000000034 method Methods 0.000 claims 11
• 125000003118 aryl group Chemical group 0.000 claims 7
• 239000003795 chemical substances by application Substances 0.000 claims 5
• 125000003545 alkoxy group Chemical group 0.000 claims 3
• 125000000217 alkyl group Chemical group 0.000 claims 3
• 125000003710 aryl alkyl group Chemical group 0.000 claims 3
• 125000004104 aryloxy group Chemical group 0.000 claims 3
• 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 3
• 239000000203 mixture Substances 0.000 claims 3
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
• BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 2
• 125000002102 aryl alkyloxo group Chemical group 0.000 claims 2
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
• 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 1
• NLYZUCJDIZZYLC-UHFFFAOYSA-N bis(2-benzoylphenyl) carbonate Chemical compound C=1C=CC=C(C(=O)C=2C=CC=CC=2)C=1OC(=O)OC1=CC=CC=C1C(=O)C1=CC=CC=C1 NLYZUCJDIZZYLC-UHFFFAOYSA-N 0.000 claims 1
• 230000000903 blocking effect Effects 0.000 claims 1
• 150000004650 carbonic acid diesters Chemical class 0.000 claims 1
• 238000006243 chemical reaction Methods 0.000 claims 1
• 150000001875 compounds Chemical class 0.000 claims 1
• 239000007822 coupling agent Substances 0.000 claims 1
• 239000000155 melt Substances 0.000 claims 1
• 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 1
• 150000002989 phenols Chemical class 0.000 claims 1
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
• 125000006678 phenoxycarbonyl group Chemical group 0.000 claims 1
• UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 1
• 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
• 238000005809 transesterification reaction Methods 0.000 claims 1