1,3,5-Triazine, 2-chloro-4,6-bis(dodecyloxy)- → HCID 22764376, compound

HRID 1112480Notes

Reaction equation

HRID 1112480 reaction equation
Cl[C:2]1[N:7]=[C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[N:5]=[C:4]([O:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45])[N:3]=1.ClC1N=C(OCCCCCCCCCCCC)N=C(OCCCCCCCCCCCC)N=1.[C:79]1([C:85]2[CH:91]=[C:90]([OH:92])[CH:89]=[C:88]([C:93]3[CH:98]=[CH:97][CH:96]=[CH:95][CH:94]=3)[C:86]=2[OH:87])[CH:84]=[CH:83][CH:82]=[CH:81][CH:80]=1>>[OH:87][C:86]1[C:85]([C:79]2[CH:84]=[CH:83][CH:82]=[CH:81][CH:80]=2)=[CH:91][C:90]([O:92][C:2]2[N:7]=[C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[N:5]=[C:4]([O:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH3:45])[N:3]=2)=[CH:89][C:88]=1[C:93]1[CH:94]=[CH:95][CH:96]=[CH:97][CH:98]=1

Participants

4

Reactant 3

HCID 5906441,3,5-Triazine, 2-chloro-4,6-bis(dodecyloxy)-HCID 10563427[1,1':3',1''-Terphenyl]-2',5'-diolHCID 142363812-Chloro-4,6-bis(octadecyloxy)-1,3,5-triazine

Product 1

HCID 22764376HCID 22764376, compound

Procedure

The preparation of the 2-chloro-4,6-distearoxy-s-triazine was carried out in the manner indicated for the 2-chlor-4,6-dilauroxy-s-triazine in Example I. Also the addition reaction with 2,6-diphenyl hydroquinone was also performed in the same manner as Examples I and II. The resulting reaction product had a melting point of 33° C.

Workup

  1. customThe resulting reaction product

Sources & evidence

ORD record
ord-480aff825f1740098ba9a0be83416c6e
Source dataset
uspto-grants-1978_10
Patent number
US04122270

Reaction notes

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