3,5-Di-tert-butylphenol → HCID 15067986, compound

HRID 1074278Notes

Reaction equation

HRID 1074278 reaction equation
Br[CH2:2][C:3]1[C:4]([C:9]#[N:10])=[CH:5][CH:6]=[CH:7][CH:8]=1.[C:11]([C:15]1[CH:16]=[C:17]([OH:25])[CH:18]=[C:19]([C:21]([CH3:24])([CH3:23])[CH3:22])[CH:20]=1)([CH3:14])([CH3:13])[CH3:12]>>[C:21]([C:19]1[CH:18]=[C:17]([CH:16]=[C:15]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:20]=1)[O:25][CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]#[N:10])([CH3:24])([CH3:23])[CH3:22]

Participants

3

Reactant 2

HCID 708253,5-Di-tert-butylphenolHCID 895992-(Bromomethyl)benzonitrile

Product 1

HCID 15067986HCID 15067986, compound

Procedure

Using the method of Example 1, 20.6 g (0.10 mole) of alpha-bromo-o-tolunitrile was reacted with 3,5-di-t-butylphenol to give 9.9 g of white crystalline 2-(3,5-di-t-butylphenoxymethyl)-1-benzenecarbonitrile.

Sources & evidence

ORD record
ord-d45b7434ac0e48eb9f6a51a753fc4e7e
Source dataset
uspto-grants-1990_11
Patent number
US04973731

Reaction notes

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