3,5-Di-tert-butyl-4-hydroxybenzaldehyde → HCID 54060698, compound

HRID 1351450Notes

Reaction equation

HRID 1351450 reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])[CH:8]=O)([CH3:4])([CH3:3])[CH3:2].[C:18]1([CH2:24][CH2:25][CH2:26][NH:27][C:28](=[O:32])[CH2:29][C:30]#[N:31])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:14]([C:11]1[CH:10]=[C:7]([CH:8]=[C:29]([C:28]([NH:27][CH2:26][CH2:25][CH2:24][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)=[O:32])[C:30]#[N:31])[CH:6]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[C:12]=1[OH:13])([CH3:17])([CH3:16])[CH3:15]

Participants

3

Reactant 2

HCID 732193,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 42956972-cyano-N-(3-phenylpropyl)acetamide

Product 1

HCID 54060698HCID 54060698, compound

Procedure

M20 was prepared using 3,5-di-t-butyl-4-hydroxybenzaldehyde and N-3-phenyl-n-propyl cyanoacetamide under the similar conditions as descibed for M21 infra.

Workup

  1. customM20 was prepared

Sources & evidence

ORD record
ord-f89d968cc9184bde8f7b82ee510c6196
Source dataset
uspto-grants-2007_05
Patent number
US07217737B2

Reaction notes

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