Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

Base Information

Chemical Name:Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate
CAS No.:136006-39-8
Molecular Formula:C₂₅H₂₁Cl₂F₂O₅*Na
Molecular Weight:533.331
Hs Code.:

Synonyms:Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

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Chemical Property of Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

Chemical Property:

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Technology Process of Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

There total 13 articles about Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate 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:

: 110705-84-5
(4R,6S)-6-{2-[Bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxymethyl}-4-hydroxy-tetrahydro-pyran-2-one

: 136006-39-8
Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

Guidance literature:: With sodium hydroxide; In ethanol; at 20 - 25 ℃; for 1h;
DOI:10.1021/jm00114a004

Reference yield:

: 403-43-0
4-fluorobenzoyl chloride

: 136006-39-8
Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

Guidance literature:: Multi-step reaction with 9 steps

1: 99 percent / NaOH / H₂O / 0.5 h

2: 81 percent / AlCl₃ / 2 h / 150 °C

3: 85 percent / tetrahydrofuran

4: 74 percent / H₂, conc. HCl / 10percent Pd/C / acetic acid / 1.5 h / 25 °C / 750.06 Torr

5: K₂CO₃, hydroquinone / dimethylsulfoxide / 3 h / 70 °C

6: glacial acetic acid / tetrahydrofuran / 72 h / Heating

7: CrO₃, pyridine, Celite / CH₂Cl₂ / 1 h / 20 - 25 °C

8: 84 percent / glacial acetic acid, tetra-n-butylammonium fluoride trihydrate / tetrahydrofuran / 4 h / 20 °C

9: 1N NaOH / ethanol / 1 h / 20 - 25 °C

With pyridine; chromium(VI) oxide; hydrogenchloride; sodium hydroxide; aluminium trichloride; Celite; tetrabutyl ammonium fluoride; hydrogen; potassium carbonate; acetic acid; hydroquinone; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; water; acetic acid; dimethyl sulfoxide;
DOI:10.1021/jm00114a004

Reference yield:

: 114865-95-1
(3,5-dichloro-2-hydroxyphenyl)-(4-fluorophenyl)methanone

: 136006-39-8
Sodium; (3R,5S)-6-{2-[bis-(4-fluoro-phenyl)-methyl]-4,6-dichloro-phenoxy}-3,5-dihydroxy-hexanoate

Guidance literature:: Multi-step reaction with 7 steps

1: 85 percent / tetrahydrofuran

2: 74 percent / H₂, conc. HCl / 10percent Pd/C / acetic acid / 1.5 h / 25 °C / 750.06 Torr

3: K₂CO₃, hydroquinone / dimethylsulfoxide / 3 h / 70 °C

4: glacial acetic acid / tetrahydrofuran / 72 h / Heating

5: CrO₃, pyridine, Celite / CH₂Cl₂ / 1 h / 20 - 25 °C

6: 84 percent / glacial acetic acid, tetra-n-butylammonium fluoride trihydrate / tetrahydrofuran / 4 h / 20 °C

7: 1N NaOH / ethanol / 1 h / 20 - 25 °C

With pyridine; chromium(VI) oxide; hydrogenchloride; sodium hydroxide; Celite; tetrabutyl ammonium fluoride; hydrogen; potassium carbonate; acetic acid; hydroquinone; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; acetic acid; dimethyl sulfoxide;
DOI:10.1021/jm00114a004