Reaction equation
C(O[C:6]1[C:19](C)=[C:18](C)[C:17]2[O:16][C:15]3[C:10](=[C:11](C)[C:12](OCC4OC4)=[C:13](C)[C:14]=3C)[CH:9](C3C=CC=CC=3)[C:8]=2[C:7]=1C)C1OC1.C(OC1C=CC(C2C=CC(OCC3OC3)=CC=2)=CC=1)C1OC1.OC1C=CC(C2C=CC(O)=CC=2)=CC=1.[OH:73][C:74]1[CH:79]=[CH:78][C:77]([C:80]([C:83]2[CH:88]=[CH:87][C:86]([OH:89])=[CH:85][CH:84]=2)([CH3:82])[CH3:81])=[CH:76][CH:75]=1>>[CH:11]1[C:10]2[CH2:9][C:8]3[C:17](=[CH:18][CH:19]=[CH:6][CH:7]=3)[O:16][C:15]=2[CH:14]=[CH:13][CH:12]=1.[OH:73][C:74]1[CH:75]=[CH:76][C:77]([C:80]([C:83]2[CH:84]=[CH:85][C:86]([OH:89])=[CH:87][CH:88]=2)([CH3:82])[CH3:81])=[CH:78][CH:79]=1Participants
5
Procedure
In the same manner as in Synthesis Example 3, except that 1.555 g (manufactured by DAINIPPON INK & CHEMICALS Co., Ltd., “EXA7335”, 3.2 mmol) of 2,7-diglycidyloxy-1,3,4,5,6,8-hexamethyl-9-phenylxanthene, 0.238 g (0.8 mmol) of 4,4′-diglycidyloxybiphenyl and 0.67 g (3.6 mmol) of 4,4′-dihydroxybiphenyl, were replaced by 1.944 g (manufactured by DAINIPPON INK & CHEMICALS Co., Ltd., “EXA7335”, 4.0 mmol) of 2,7-diglycidyloxy-1,3,4,5,6,8-hexamethyl-9-phenylxanthene and 0.821 g (3.6 mmol) of bisphenol A, a xanthene-bisphenol A copolymer type linear epoxy resin was obtained. The amount of the resulting xanthene-bisphenol A copolymer type linear epoxy resin was 2.69 g and the yield was 97%.
Workup
- customIn the same manner as in Synthesis Example 3
Sources & evidence
- ORD record
- ord-42b9c316a8d44f4fafd0513fdd430a40
- Source dataset
- uspto-grants-2009_04
- Patent number
- US07514507B2
Linked notes
Loading…