2,4,6-Tri-tert-butylphenol → HCID 19438417, compound

HRID 1734773Notes

Reaction equation

HRID 1734773 reaction equation
Cl[P:2]1[N:5]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)[P:4](Cl)[N:3]1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.[C:19]([C:23]1[CH:28]=[C:27]([C:29]([CH3:32])([CH3:31])[CH3:30])[CH:26]=[C:25]([C:33]([CH3:36])([CH3:35])[CH3:34])[C:24]=1[OH:37])([CH3:22])([CH3:21])[CH3:20]>C(N(CC)CC)C>[C:19]([C:23]1[CH:28]=[C:27]([C:29]([CH3:32])([CH3:31])[CH3:30])[CH:26]=[C:25]([C:33]([CH3:36])([CH3:35])[CH3:34])[C:24]=1[O:37][P:2]1[N:5]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=2)[P:4]([O:37][C:24]2[C:25]([C:33]([CH3:34])([CH3:35])[CH3:36])=[CH:26][C:27]([C:29]([CH3:32])([CH3:31])[CH3:30])=[CH:28][C:23]=2[C:19]([CH3:22])([CH3:21])[CH3:20])[N:3]1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)([CH3:22])([CH3:21])[CH3:20]

Participants

4

Reactant 2

HCID 129022,4,6-Tri-tert-butylphenolHCID 15389826HCID 15389826, compound

Product 1

HCID 19438417HCID 19438417, compound

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

The procedure of Example 1 is repeated using 2,4-dichloro-1,3-diphenyl-1,3,2,4-diazadiphosphetidine, 2,4,6-tri-tert-butylphenol and triethylamine to give the title compound.

Sources & evidence

ORD record
ord-ef0abcdf647c41c1a8ab141ba27731fa
Source dataset
uspto-grants-1996_07
Patent number
US05534646

Reaction notes

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