(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

Base Information

Chemical Name:(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol
CAS No.:876587-30-3
Molecular Formula:C₂₁H₂₄F₄O₂S
Molecular Weight:416.48
Hs Code.:

Synonyms:(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

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Chemical Property of (R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

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Technology Process of (R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

There total 3 articles about (R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol 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: 100.0%

: 866943-83-1
(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-((R)-toluene-4-sulfinylmethyl)pentan-2-ol

: 876587-30-3
(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

Guidance literature:: With trifluoroacetic anhydride; sodium iodide; In acetone; at -40 ℃;
DOI:10.1016/j.bmcl.2005.10.039

Reference yield:

: 609806-82-8
1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methylpentan-2-one

: 876587-30-3
(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium diisopropylamide / tetrahydrofuran; cyclohexane / 0.25 h / -78 °C

1.2: 29 percent / tetrahydrofuran; cyclohexane / 1.5 h / -78 °C

2.1: 100 percent / NaI; trifluoroacetic anhydride / acetone / -40 °C

With trifluoroacetic anhydride; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; acetone;
DOI:10.1016/j.bmcl.2005.10.039

Reference yield:

: 1519-39-7
(R)-methyl p-tolyl sulfoxide

: 876587-30-3
(R)-1,1,1-trifluoro-4-(5-fluoro-2-methoxyphenyl)-4-methyl-2-(p-tolylsulfanylmethyl)pentan-2-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: lithium diisopropylamide / tetrahydrofuran; cyclohexane / 0.25 h / -78 °C

1.2: 29 percent / tetrahydrofuran; cyclohexane / 1.5 h / -78 °C

2.1: 100 percent / NaI; trifluoroacetic anhydride / acetone / -40 °C

With trifluoroacetic anhydride; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; cyclohexane; acetone;
DOI:10.1016/j.bmcl.2005.10.039