Cyanuric chloride → 1,3,5-Triazine, 2,4,6-tris(2,3,4,5,6-pentabromophenoxy)-

HRID 1605211Notes

Reaction equation

[Br:1][C:2]1[C:7]([OH:8])=[C:6]([Br:9])[C:5]([Br:10])=[C:4]([Br:11])[C:3]=1[Br:12].[N:13]1[C:20](Cl)=[N:19][C:17](Cl)=[N:16][C:14]=1Cl>>[Br:1][C:2]1[C:7]([O:8][C:14]2[N:16]=[C:17]([O:8][C:7]3[C:2]([Br:1])=[C:3]([Br:12])[C:4]([Br:11])=[C:5]([Br:10])[C:6]=3[Br:9])[N:19]=[C:20]([O:8][C:7]3[C:6]([Br:9])=[C:5]([Br:10])[C:4]([Br:11])=[C:3]([Br:12])[C:2]=3[Br:1])[N:13]=2)=[C:6]([Br:9])[C:5]([Br:10])=[C:4]([Br:11])[C:3]=1[Br:12]

Participants

Reactant 2

HCID 7954Cyanuric chloride

HCID 11852Pentabromophenol

Product 1

HCID 1047061,3,5-Triazine, 2,4,6-tris(2,3,4,5,6-pentabromophenoxy)-

Procedure

Tris-(pentabromophenoxy)-s-triazine was prepared from pentabromophenol and cyanuric chloride using the process described in Example 1, above. The compound was found to have a melting point of 320°-325°C.

Sources & evidence

ORD record: ord-34565b9befc1453892a90b23fd6db8d0
Source dataset: uspto-grants-1976_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US03950306

Reaction notes

Loading…