US2020031986A1PendingUtilityA1
Polyol or polythiol compound, preparation method therefor, transparent polyurethane-based resin prepared therefrom, and optical body
Est. expiryFeb 15, 2037(~10.6 yrs left)· nominal 20-yr term from priority
Inventors:Keun Sik Kim
C08L 75/04C08G 18/755C08G 18/758C08G 18/7642C08G 18/752C08G 18/3876C08G 18/7831G02B 1/041C08G 18/72C07C 323/12G02C 7/02C07C 321/04B29D 11/00G02B 1/04C07C 319/08C08G 18/38C08G 18/757C08G 18/73C08G 18/242C08G 18/24C07C 321/14C07C 319/20C07C 319/14B29K 2075/00C07C 323/03C08G 18/3855
55
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention relates to a novel polyol or polythiol having three or more functional groups, a preparation method there for, and an optical body manufactured therefrom. Especially, the present invention relates to a poly(thio)urethane-based resin and an optical body, such as lenses, manufactured using the resin, wherein the poly(thio)urethane-based resin is prepared by obtaining a novel polyol and then combining a polythiol, which is prepared from the obtained polyol, with a polyiso(thio)cyanate.
Claims
exact text as granted — not AI-modified1 - 23 . (canceled)
24 . A polyol or polythiol compound or an isomer thereof, the polyol or polythiol compound having at least three functional groups and represented by Formula (a) or (b):
(where Y is an oxygen atom or a sulfur atom;
Ra is a lower alkyl group;
i) for the polyol, Rb is —CH 2 CH(OH)CH 2 F, —CH 2 CH(OH)CH 2 Cl, —CH 2 CH(OH)CH 2 Br, —CH 2 CH(OH)CH 2 I,
—CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 3 ,
—CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH(CH 3 )CH 2 OH,
—CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 3 ,
—CH 2 CH(OH)CH 2 SCH(CH 3 )CH 2 OH,
—CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 CH 3 ,
—CH 2 CH(OH)CH 2 SCH(CH 2 CH 3 )CH 2 OH,
—CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 CH 3 , or
—CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH(CH 2 CH 3 )CH 2 OH;
ii) for the polythiol, Rb is —CH(CH 2 SH)CH 2 SH,
—CH 2 CH(CH 2 SH)SCH(CH 3 )CH 2 SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 3 )SH,
—CH(CH 2 SH)CH 2 SCH(CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 3 )SH,
—CH 2 CH(CH 2 SH)SCH(CH 2 CH 3 )CH 2 SH,
—CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 CH 3 )SH,
—CH(CH 2 SH)CH 2 SCH(CH 2 CH 3 )CH 2 SH,
—CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 CH 3 )SH,
—CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH(CH 3 )CH 2 SH,
—CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH 2 CH(CH 3 )SH,
—CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH(CH 3 )CH 2 SH,
—CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH 2 CH(CH 3 )SH,
—CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH(CH 3 )CH 2 SH,
—CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH 2 CH(CH 3 )SH,
—CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH(CH 3 )CH 2 SH,
—CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH 2 CH(CH 3 )SH,
—CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH(CH 2 CH 3 )CH 2 SH,
—CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH 2 CH(CH 2 CH 3 )SH,
—CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH(CH 2 CH 3 )CH 2 SH,
—CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH 2 CH(CH 2 CH 3 )SH,
—CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH(CH 2 CH 3 )CH 2 SH,
—CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH 2 CH(CH 2 CH 3 )SH,
—CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH(CH 2 CH 3 )CH 2 SH, or
—CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH 2 CH(CH 2 CH 3 )SH).
25 . The polyol compound according to claim 24 , as represented by Formula (a) or (b), wherein Y is an oxygen atom; Ra is a methyl or ethyl group; and Rb is one substituent selected from the group consisting of the following substituents:
—CH 2 CH(OH)CH 2 F, —CH 2 CH(OH)CH 2 Cl, —CH 2 CH(OH)CH 2 Br, —CH 2 CH(OH)CH 2 I, —CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 3 , —CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH(CH 3 )CH 2 OH, —CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 3 , —CH 2 CH(OH)CH 2 SCH(CH 3 )CH 2 OH, —CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 CH 3 , —CH 2 CH(OH)CH 2 SCH(CH 2 CH 3 )CH 2 OH, —CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 CH 3 , and —CH 2 CH(OH)CH 2 SCH 2 CH(OH)CH 2 SCH(CH 2 CH 3 )CH 2 OH.
26 . The polythiol compound according to claim 24 , as represented by Formula (a) or (b), wherein Y is a sulfur atom; Ra is a methyl or ethyl group; and Rb is one substituent selected from the group consisting of the following substituents:
—CH(CH 2 SH)CH 2 SH, —CH 2 CH(CH 2 SH)SCH(CH 3 )CH 2 SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 3 )SH, —CH(CH 2 SH)CH 2 SCH(CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 3 )SH, —CH 2 CH(CH 2 SH)SCH(CH 2 CH 3 )CH 2 SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 CH 3 )SH, —CH(CH 2 SH)CH 2 SCH(CH 2 CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 CH 3 )SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH(CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH 2 CH(CH 3 )SH, —CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH(CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH 2 CH(CH 3 )SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH(CH 3 )CH 2 SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH 2 CH(CH 3 )SH, —CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH(CH 3 )CH 2 SH, —CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH 2 CH(CH 3 )SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH(CH 2 CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH 2 CH(CH 2 SH)SCH 2 CH(CH 2 CH 3 )SH, —CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH(CH 2 CH 3 )CH 2 SH, —CH(CH 2 SH)CH 2 SCH(CH 2 SH)CH 2 SCH 2 CH(CH 2 CH 3 )SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH(CH 2 CH 3 )CH 2 SH, —CH 2 CH(CH 2 SH)SCH 2 CH(CH 2 SH)SCH 2 CH(CH 2 CH 3 )SH, —CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH(CH 2 CH 3 )CH 2 SH, and —CH 2 CH(CH 2 SH)SCH(CH 2 SH)CH 2 SCH 2 CH(CH 2 CH 3 )SH.
27 . A poly(thio)urethane resin composition comprising the polythiol compound having at least three functional groups according to claim 24 and a polyisocyanate.
28 . A poly(thio)urethane resin composition comprising the polythiol compound having at least three functional groups according to claim 26 and a polyisocyanate.
29 . The poly(thio)urethane resin composition according to claim 27 , wherein a mole ratio (NCO/SH) of a functional group (—NCO) of the polyisocyanate to a functional group (—SH) of the polythiol compound is in the range of 0.8 to 1.3.
30 . The poly(thio)urethane resin composition according to claim 28 , wherein a mole ratio (NCO/SH) of a functional group (—NCO) of the polyisocyanate to a functional group (—SH) of the polythiol compound is in the range of 0.8 to 1.3.
31 . The poly(thio)urethane resin composition according to claim 27 , the poly(thio)urethane resin composition is used as a plastic optical body.
32 . The poly(thio)urethane resin composition according to claim 28 , the poly(thio)urethane resin composition is used as a plastic optical body.
33 . The poly(thio)urethane resin composition according to claim 29 , the poly(thio)urethane resin composition is used as a plastic optical body.
34 . The poly(thio)urethane resin composition according to claim 30 , the poly(thio)urethane resin composition is used as a plastic optical body.
35 . The poly(thio)urethane-based plastic optical body according to claim 33 , wherein the plastic optical body is optical glasses or an optical lens.
36 . The poly(thio)urethane-based plastic optical body according to claim 34 , wherein the plastic optical body is optical glasses or an optical lens.Join the waitlist — get patent alerts
Track US2020031986A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.