[(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

Base Information

Chemical Name:[(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene
CAS No.:114969-28-7
Molecular Formula:C₂₀H₂₅FO₂S
Molecular Weight:348.482
Hs Code.:

Synonyms:[(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

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Chemical Property of [(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

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Technology Process of [(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

There total 2 articles about [(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene 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:

: 56069-39-7
diethyl phenylsulfonylmethylphosphonate

: 114969-28-7
[(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) KH; 2.) FClO₃ (g) / 1.) THF, 0-15 deg C, 2 h; 2.) 0.5-1 h

2: 1.) NaH / 1.) TFH, -70 deg C, 2 h; 2.) 0 deg C, 1-2 h

With perchloryl fluoride; potassium hydride; sodium hydride;

Reference yield:

: 79-77-6,14901-07-6
(E)-β-ionone

: 135789-87-6,114968-97-7
phosphonic acid diethyl ester

: 114969-29-8
[(1Z,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

: 114969-28-7
[(1E,3E)-1-Fluoro-2-methyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-buta-1,3-diene-1-sulfonyl]-benzene

Guidance literature:: With sodium hydride; Yield given. Multistep reaction. Yields of byproduct given; 1.) TFH, -70 deg C, 2 h; 2.) 0 deg C, 1-2 h;