Production Method 1

141-82-2

86-81-7

13400-02-7

90-50-6

Reaction Conditions

1.1 Reagents: Piperidine Solvents: Acetic acid ;  8 min, 130 °C

Reference

One-pot two-step synthesis of 4-vinylphenols from 4-hydroxy substituted benzaldehydes under microwave irradiation: a new perspective on the classical Knoevenagel-Doebner reaction

Sinha, Arun K.; et al, Tetrahedron, 2007, 63(4), 960-965

5-ethenyl-1,2,3-trimethoxybenzene Raw materials

• propanedioic acid
• 3,4,5-Trimethoxybenzaldehyde

5-ethenyl-1,2,3-trimethoxybenzene Preparation Products

• 5-ethenyl-1,2,3-trimethoxybenzene (13400-02-7)
• 3,4,5-Trimethoxycinnamic acid (90-50-6)

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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenol ethers Anisoles

• 97-54-1(Isoeugenol)
• 7786-61-0(2-Methoxy-4-vinylphenol)
• 93-16-3(Methyl isoeugenol)
• 117048-59-6(Combretastatin A4)
• 32507-66-7(isorhapontigenin)
• 28343-22-8(4-Vinylsyringol)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)