3,5-Di-tert-butylphenol → HCID 15067990, compound

HRID 1074280Notes

Reaction equation

HRID 1074280 reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([C:9]#[N:10])[CH:4]=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:4]=[C:5]([C:9]#[N:10])[CH:6]=[CH:7][CH:8]=1)([CH3:24])([CH3:23])[CH3:22]

Participants

3

Reactant 2

HCID 708253,5-Di-tert-butylphenolHCID 97249Benzonitrile, 3-(bromomethyl)-

Product 1

HCID 15067990HCID 15067990, compound

Procedure

Using the method of Example 1, 20.6 g (0.10 mole) of alpha-bromo-m-tolunitrile was reacted with 3,5-di-t-butylphenol to give white crystalline 3-(3,5-di-t-butylphenoxymethyl)-1-benzenecarbonitrile. Analysis: Calculated for C22H27NO: %C 82.2; %H, 8.4; %N, 4.4; Found: %C, 82.2; H, 8.5; %N, 4.1.

Sources & evidence

ORD record
ord-f905bd82f6934c8a861d56243c0472b9
Source dataset
uspto-grants-1990_11
Patent number
US04973731

Reaction notes

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