3,5-Dimethyl-4-hydroxybenzaldehyde → (E)-3-(3,5-Dimethyl-4-hydroxyphenyl)2-[(3-phenyl-n-propyl)aminosulfonyl]acrylonitrile

HRID 481479Notes

Reaction equation

HRID 481479 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([CH3:11])[C:9]=1[OH:10])[CH:5]=O.[C:12]1([CH2:18][CH2:19][CH2:20][NH:21][S:22]([CH2:25][C:26]#[N:27])(=[O:24])=[O:23])[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[CH3:1][C:2]1[CH:3]=[C:4](/[CH:5]=[C:25](/[S:22]([NH:21][CH2:20][CH2:19][CH2:18][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)(=[O:24])=[O:23])\[C:26]#[N:27])[CH:7]=[C:8]([CH3:11])[C:9]=1[OH:10]

Participants

3

Reactant 2

HCID 752223,5-Dimethyl-4-hydroxybenzaldehydeHCID 15410494(3-Phenyl-n-propyl)aminosulfonylacetonitrile

Product 1

HCID 15516465(E)-3-(3,5-Dimethyl-4-hydroxyphenyl)2-[(3-phenyl-n-propyl)aminosulfonyl]acrylonitrile

Procedure

M45 was prepared with 3,5-dimethyl-4-hydroxybenzaldehyde and N-3-phenyl-n-propyl cyanomethylsulfonamide under similar conditions as described for M40 (part B).

Sources & evidence

ORD record
ord-4f3afc9d157c497eb1a25f58ad6b5106
Source dataset
uspto-grants-1998_08
Patent number
US05789427

Reaction notes

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