3,5-Di-tert-butyl-4-hydroxybenzaldehyde → HCID 9968867, compound

HRID 965252Notes

Reaction equation

HRID 965252 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].[S:18]([CH2:24][C:25]#[N:26])([CH2:21][C:22]#[N:23])(=[O:20])=[O:19]>>[C:1]([C:5]1[CH:6]=[C:7](/[CH:8]=[C:21](/[S:18]([CH2:24][C:25]#[N:26])(=[O:20])=[O:19])\[C:22]#[N:23])[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 142163Sulphonyl diacetonitrile

Product 1

HCID 9968867HCID 9968867, compound

Procedure

M36 was prepared with 3,5-di-t-butyl-4-hydroxybenzaldehyde and sulfonyl diacetonitrile under similar conditions as described for M27.

Sources & evidence

ORD record
ord-77d19ad75c304fcca1e3317e67681e55
Source dataset
uspto-grants-1998_06
Patent number
US05773476

Reaction notes

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