2,6-Di-tert-butylphenol → HCID 178506936, compound

HRID 966141Notes

Reaction equation

HRID 966141 reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][CH:8]=[C:7]([C:11]([CH3:14])([CH3:13])[CH3:12])[C:6]=1[OH:15])([CH3:4])([CH3:3])[CH3:2].C([Li:20])CCC>C1(C)C=CC=CC=1>[C:11]([C:7]1[CH:8]=[CH:9][CH:10]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[C:6]=1[O:15][Li:20])([CH3:14])([CH3:13])[CH3:12]

Participants

4

Reactant 2

HCID 314052,6-Di-tert-butylphenolHCID 178418339Butyllithium

Product 1

HCID 178506936HCID 178506936, compoundYield 95%

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Both 10 mmol (2.2 g) of monocyclopentadienyl titanium chloride(CpTiCl3) and 100 ml of toluene were added to a 200 ml Schlenk reactor in the atmosphere of inert gas. Then, 10 mmol of 2,6-di-t-butyl phenoxy lithium, so obtained from the reaction between 2,6-di-t-butyl phenol and n-butyl lithium, was slowly added to the mixture. The reactional solution was stirred at room temperature and stood for 1 hour. After 1 hour, some mixture was collected and was analyzed by 1H-NMR spectroscopy to ascertain the reaction results.

Sources & evidence

ORD record
ord-825542a0640a46dc976ba23e774e3bcd
Source dataset
uspto-grants-2005_10
Patent number
US06951906B1

Reaction notes

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