(-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

Base Information

Chemical Name:(-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate
CAS No.:383191-61-5
Molecular Formula:C₂₆H₃₈O₈
Molecular Weight:478.583
Hs Code.:

Synonyms:(-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

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Chemical Property of (-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

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Technology Process of (-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

There total 2 articles about (-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate 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: 68.0%

: 321146-37-6
(-)-(1R,6R)-6-hydroxy-4-[[(4R,6S)-6-[(2S)-4-hydroxy-2-[(4-methoxybenzoyl)oxy]butyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

: 383191-61-5
(-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

: (-)-(1R,6R)-6-hydroxy-4-[[(4R,6S)-6-[(2S)-4-[(4-methoxybenzoyl)oxy]-2-hydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

Guidance literature:: With magnesium methanolate; In methanol; at 40 ℃; for 8h;
DOI:10.1021/jo010172u

Reference yield:

: 321146-33-2
(1R,6R)-6-Hydroxy-4-{(2R,4S,6S)-2,4,8-trihydroxy-6-[(4-methoxybenzoyl)oxy]octyl}cyclohept-1-en-1-yl 4-methoxybenzoate

: 383191-61-5
(-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / PPTS / acetone / 4 h / 0 °C

2: 68 percent / Mg(OMe)2 / methanol / 8 h / 40 °C

With pyridinium p-toluenesulfonate; magnesium methanolate; In methanol; acetone;
DOI:10.1021/jo010172u

Reference yield:

: 383191-61-5
(-)-(1R,6R)-6-hydroxy-4-[[(4R,6R)-6-[(2S)-2,4-dihydroxybutyl]-2,2-dimethyl-1,3-dioxan-4-yl]methyl]cyclohept-3-en-1-yl 4-methoxybenzoate

: 4-Methoxy-benzoic acid (1S,6S)-4-[(4S,6R)-6-((S)-2,4-dihydroxy-butyl)-2,2-dimethyl-[1,3]dioxan-4-ylmethyl]-3,4,6-trihydroxy-cycloheptyl ester

Guidance literature:: With osmium(VIII) oxide; N-methyl-2-indolinone; In tetrachloromethane; water; acetone; at 20 ℃; for 15h;
DOI:10.1021/jo010172u