5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

Base Information

Chemical Name:5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one
CAS No.:138958-35-7
Molecular Formula:C₁₆H₁₅ClO₂
Molecular Weight:274.747
Hs Code.:

Synonyms:5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

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Chemical Property of 5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

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Technology Process of 5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

There total 3 articles about 5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one 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: 36.0%

: 1559-45-1
2,2,5-trimethyl-3(2H)-furanone

: 1075-77-0
4-chlorocinnamaldehyde

: 138958-35-7
5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

Guidance literature:: With sodium hydroxide; In ethanol; for 16h; Ambient temperature;
DOI:10.1021/jm00085a003

Reference yield:

: 138958-55-1
2-(3-methyl-5-isoxazolyl)-2-propanol

: 138958-35-7
5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) H₂, 2.) 1N aq. HCl / 1.) 10percent Pd/C / 1.) CH₃OH, 30 psi, 2.) H₂O, 2 h

2: 36 percent / 1 N aq. NaOH / ethanol / 16 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; palladium on activated charcoal; In ethanol;
DOI:10.1021/jm00085a003

Reference yield:

: 115-19-5
2-methyl-but-3-yn-2-ol

: 138958-35-7
5-[(1E,3E)-4-(4-Chloro-phenyl)-buta-1,3-dienyl]-2,2-dimethyl-furan-3-one

Guidance literature:: Multi-step reaction with 3 steps

1: 49.7 percent / Et₃N, POCl₃ / CHCl₃ / Ambient temperature

2: 1.) H₂, 2.) 1N aq. HCl / 1.) 10percent Pd/C / 1.) CH₃OH, 30 psi, 2.) H₂O, 2 h

3: 36 percent / 1 N aq. NaOH / ethanol / 16 h / Ambient temperature

With hydrogenchloride; sodium hydroxide; hydrogen; triethylamine; trichlorophosphate; palladium on activated charcoal; In ethanol; chloroform;
DOI:10.1021/jm00085a003