Dimethyl-2,6-naphthalenedicarboxylate → 2,6-Naphthalenedicarboxylic acid

HRID 1877735Notes

Reaction equation

HRID 1877735 reaction equation
[CH:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([O:13]C)=[O:12])=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:15]([O:17]C)=[O:16].[CH2:19]([CH2:34][O:35][C:36]1[CH:37]=[C:38]2[C:43](=[CH:44][CH:45]=1)[CH:42]=[C:41]([C:46]([OH:48])=[O:47])[CH:40]=[CH:39]2)[O:20][C:21]1[CH:22]=[C:23]2[C:28](=[CH:29][CH:30]=1)[CH:27]=[C:26]([C:31]([OH:33])=[O:32])[CH:25]=[CH:24]2>[O-]CCCC.[O-]CCCC.[O-]CCCC.[O-]CCCC.[Ti+4].C(O)CO>[CH:1]1[C:10]2[C:5](=[CH:6][C:7]([C:11]([OH:13])=[O:12])=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:15]([OH:17])=[O:16].[CH2:34]([CH2:19][O:20][C:21]1[CH:22]=[C:23]2[C:28](=[CH:29][CH:30]=1)[CH:27]=[C:26]([C:31]([OH:33])=[O:32])[CH:25]=[CH:24]2)[O:35][C:36]1[CH:37]=[C:38]2[C:43](=[CH:44][CH:45]=1)[CH:42]=[C:41]([C:46]([OH:48])=[O:47])[CH:40]=[CH:39]2

Participants

6

Procedure

Further, an esterification reaction and a transesterification reaction were carried out among dimethyl 2,6-naphthalenedicarboxylate, 6,6′-(ethylenedioxy)di-2-naphthoic acid and ethylene glycol in the presence of titanium tetrabutoxide and then a polycondensation reaction was carried out to obtain an aromatic polyester (B-1) for the film layer (B) which comprised 73 mol % of a 2,6-naphthalenedicarboxylic acid component and 27 mol % of a 6,6′-(ethylenedioxy)di-2-naphthoic acid component based on the total of all the acid components and 98 mol % of an ethylene glycol component and 2 mol % of a diethylene glycol component based on the total of all the glycol components. 0.15 wt % of silica particles having an average particle diameter of 0.3 μm and 0.10 wt % of silica particles having an average particle diameter of 0.15 μm were contained in the aromatic polyester (B-1) based on the weight of the resin composition obtained before the polycondensation reaction. This aromatic polyester (B-1) had a melting point of 240° C. and a glass transition temperature of 117° C.

Workup

  1. customFurther, an esterification reaction
  2. customa transesterification reaction
  3. customa polycondensation reaction

Sources & evidence

ORD record
ord-20015ad518f3401fa9b424451460d702
Source dataset
uspto-grants-2012_11
Patent number
US08313849B2

Reaction notes

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