Phenylsulphonylacetonitrile → HCID 9885663, compound

HRID 1351455Notes

Reaction equation

HRID 1351455 reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([CH:9]=[C:10]([CH:13]([CH3:15])[CH3:14])[C:11]=1[OH:12])[CH:7]=O)([CH3:3])[CH3:2].[C:16]1([S:22]([CH2:25][C:26]#[N:27])(=[O:24])=[O:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH:1]([C:4]1[CH:5]=[C:6](/[CH:7]=[C:25](/[S:22]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)(=[O:23])=[O:24])\[C:26]#[N:27])[CH:9]=[C:10]([CH:13]([CH3:15])[CH3:14])[C:11]=1[OH:12])([CH3:3])[CH3:2]

Participants

3

Reactant 2

HCID 82077PhenylsulphonylacetonitrileHCID 827124-Hydroxy-3,5-bis(isopropyl)benzaldehyde

Product 1

HCID 9885663HCID 9885663, compound

Procedure

M30 was prepared with 3,5-diisopropyl-4-hydroxybenzaldehyde and phenylsulfonly acetonitrile under the similar conditions as decribed for M26.

Sources & evidence

ORD record
ord-c4377f4267c748ba98d83ff76875f745
Source dataset
uspto-grants-2007_05
Patent number
US07217737B2

Reaction notes

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