Octadecyl DI-tert-butyl-4-hydroxyhydrocinnamate → HCID 19438419, compound

HRID 1734769Notes

Reaction equation

HRID 1734769 reaction equation
Cl[P:2]1[N:5]([C:6]([CH3:9])([CH3:8])[CH3:7])[P:4](Cl)[N:3]1[C:11]([CH3:14])([CH3:13])[CH3:12].[C:15]([C:19]1[CH:20]=[C:21]([CH:45]=[C:46]([C:49]([CH3:52])([CH3:51])[CH3:50])[C:47]=1[OH:48])[CH2:22][CH2:23][C:24]([O:26][CH2:27][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][CH3:44])=[O:25])([CH3:18])([CH3:17])[CH3:16]>C(N(CC)CC)C>[C:15]([C:19]1[CH:20]=[C:21]([CH2:22][CH2:23][C:24]([O:26][CH2:27][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][CH3:44])=[O:25])[CH:45]=[C:46]([C:49]([CH3:51])([CH3:50])[CH3:52])[C:47]=1[O:48][P:2]1[N:5]([C:6]([CH3:9])([CH3:8])[CH3:7])[P:4]([O:48][C:47]2[C:19]([C:15]([CH3:18])([CH3:17])[CH3:16])=[CH:20][C:21]([CH2:22][CH2:23][C:24]([O:26][CH2:27][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][CH3:44])=[O:25])=[CH:45][C:46]=2[C:49]([CH3:50])([CH3:52])[CH3:51])[N:3]1[C:11]([CH3:14])([CH3:13])[CH3:12])([CH3:16])([CH3:17])[CH3:18]

Participants

4

Reactant 2

HCID 16386Octadecyl DI-tert-butyl-4-hydroxyhydrocinnamateHCID 125327951,3-Di-tert-butyl-2,4-dichloro-1,3,2,4-diazadiphosphetidine

Product 1

HCID 19438419HCID 19438419, compound

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

The procedure of Example 1 is repeated using 2,4-dichloro-1,3-di-tert-butyl-1,3,2,4-diazadiphosphetidine, n-octadecyl 3,5-di-tert-butyl-4-hydroxyhydrocinnamate and triethylamine to give the title compound.

Sources & evidence

ORD record
ord-3b892771e63d47c284f2bcbe597fd60e
Source dataset
uspto-grants-1996_07
Patent number
US05534646

Reaction notes

Loading…