(Z)-3-(3-nitro-4-methylphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-ene-nitrile → (E)-3-(3-nitro-4-methylphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-ene-nitrile

HRID 2903Notes

Reaction equation

HRID 2903 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6](/[CH:11]=[C:12](/[C:15]2[CH:20]=[C:19]([O:21][CH3:22])[C:18]([O:23][CH3:24])=[C:17]([O:25][CH3:26])[CH:16]=2)\[C:13]#[N:14])[CH:7]=[CH:8][C:9]=1[CH3:10])([O-:3])=[O:2]>CC(C)=O>[N+:1]([C:4]1[CH:5]=[C:6](/[CH:11]=[C:12](\[C:15]2[CH:20]=[C:19]([O:21][CH3:22])[C:18]([O:23][CH3:24])=[C:17]([O:25][CH3:26])[CH:16]=2)/[C:13]#[N:14])[CH:7]=[CH:8][C:9]=1[CH3:10])([O-:3])=[O:2]

Participants

3

Procedure

1.38 g of (Z)-3-(3-nitro-4-methylphenyl)-2-(3,4,5-trimethoxyphenyl)-prop-2-ene-nitrile was dissolved in 500 ml of acetone and the mixture was reacted in a photochemical apparatus (visible light) for 1 hour. The reaction mixture was concentrated and a quarter of it was purified on a silica gel plate to give 100 mg of the intended compound.

Workup

  1. customthe mixture was reacted in a photochemical apparatus (visible light) for 1 hour
  2. concentrationThe reaction mixture was concentrated
  3. customa quarter of it was purified on a silica gel plate

Sources & evidence

ORD record
ord-57d4b77be99049839cad797e5f680f84
Source dataset
uspto-grants-1998_03
Patent number
US05731353

Reaction notes

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