3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

Base Information

Chemical Name:3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>
CAS No.:75999-08-5
Molecular Formula:C₁₈H₂₂N₂O₂
Molecular Weight:298.385
Hs Code.:

Synonyms:3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

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Chemical Property of 3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

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Technology Process of 3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

There total 5 articles about 3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester> which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 95.0%

: 3350-78-5
3,3-Dimethylacryloyl chloride

: 75999-00-7
4-(1,3,5-trimethyl-1H-pyrazol-4-ylmethyl)phenol

: 75999-08-5
3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

Guidance literature:: With pyridine; In dichloromethane; 1) room temperature, 2 h, 2) reflux, 2 h;

Reference yield:

: 17792-58-4
2-acetyl-3-(4-hydroxyphenyl)-1-methylpropenone

: 75999-08-5
3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / H₂ / Raney-Ni / ethanol / 36 h / Ambient temperature

2: 70 percent / ethanol / 4 h / Heating

3: 95 percent / pyridine / CH₂Cl₂ / 1) room temperature, 2 h, 2) reflux, 2 h

With pyridine; hydrogen; nickel; In ethanol; dichloromethane;

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 75999-08-5
3-Methyl-2-butensaeure-<4-(1,3,5-trimethylpyrazol-4-ylmethyl)phenylester>

Guidance literature:: Multi-step reaction with 4 steps

1: 76 percent / piperidine, glacial acetic acid / benzene / 7 h / Heating

2: 98 percent / H₂ / Raney-Ni / ethanol / 36 h / Ambient temperature

3: 70 percent / ethanol / 4 h / Heating

4: 95 percent / pyridine / CH₂Cl₂ / 1) room temperature, 2 h, 2) reflux, 2 h

With piperidine; pyridine; hydrogen; acetic acid; nickel; In ethanol; dichloromethane; benzene;