Ammonia → HCID 23292951, compound

HRID 1955170Notes

Reaction equation

N[C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:5]=[C:4]([NH:13][CH2:14][CH2:15][CH2:16][CH3:17])[N:3]=1.[CH2:18]([NH2:30])[CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29].N>>[CH2:14]([NH:13][C:4]1[N:5]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:7]=[C:2]([NH:30][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH3:29])[N:3]=1)[CH2:15][CH2:16][CH3:17]

Participants

Reactant 3

HCID 222Ammonia

HCID 13583Dodecylamine

HCID 11806705HCID 11806705, compound

Product 1

HCID 23292951HCID 23292951, compound

Procedure

The same procedures were repeated as in the N-substituted melamine (C1), except that n-dodecyl amine was employed in place of the aqueous ammonia to obtain 2,4-bis(monobutyl-amino)-6-(monododecylamino)-1,3,5-triazine which is in a solid-state.

Sources & evidence

ORD record: ord-f88bf19344af4292a8c41645f0da5668
Source dataset: uspto-grants-2000_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06124381

Reaction notes

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