3,5-Di-tert-butyl-4-hydroxybenzaldehyde → HCID 1571247, compound

HRID 481473Notes

Reaction equation

HRID 481473 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([S:24]([CH2:27][C:28]#[N:29])(=[O:26])=[O:25])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:1]([C:5]1[CH:6]=[C:7](/[CH:8]=[C:27](/[S:24]([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)(=[O:25])=[O:26])\[C:28]#[N:29])[CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])([CH3:4])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 732193,5-Di-tert-butyl-4-hydroxybenzaldehydeHCID 82077Phenylsulphonylacetonitrile

Product 1

HCID 1571247HCID 1571247, compound

Procedure

M33 was prepared with 3,5-di-t-butyl-4-hydroxybenzaldehyde and phenylsulfonly acetonitrile under similar conditions as decribed for M26.

Sources & evidence

ORD record
ord-38a1781c965444029f955084653e94f3
Source dataset
uspto-grants-1998_08
Patent number
US05789427

Reaction notes

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