(4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

Base Information

Chemical Name:(4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one
CAS No.:245040-57-7
Molecular Formula:C₂₆H₃₈O₅
Molecular Weight:430.585
Hs Code.:

Synonyms:(4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

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Chemical Property of (4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

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Technology Process of (4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

There total 6 articles about (4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-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: 62.0%

: 61866-32-8
(S)-2-methyl-4-pentenal

: 245040-42-0
2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one

: 245040-57-7
(4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

: (4S,5R,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

Guidance literature:: With n-butyllithium; diisopropylamine; In tetrahydrofuran; at -78 ℃; for 0.333333h;
DOI:10.1016/S0040-4020(99)00301-4

Reference yield:

: 2186-92-7
p-Anisaldehyde dimethyl acetal

: 245040-57-7
(4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

Guidance literature:: Multi-step reaction with 2 steps

1.1: camphosulfonic acid / CH₂Cl₂ / 1 h / -78 °C

1.2: 55 percent / Dess-Martin periodinane reagent / CH₂Cl₂ / 2 h / 0 - 25 °C

2.1: 62 percent / iPr₂NH; nBuLi / tetrahydrofuran / 0.33 h / -78 °C

With n-butyllithium; camphor-10-sulfonic acid; diisopropylamine; In tetrahydrofuran; dichloromethane; 1.1: Condensation / 1.2: Oxidation / 2.1: Condensation;
DOI:10.1016/S0040-4020(99)00301-4

Reference yield:

: 128461-58-5
(4S,5R)-4-Methyl-3-(pent-4-enoyl)-5-phenyl-1,3-oxazolidin-2-one

: 245040-57-7
(4R,5S,6S)-2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-5-hydroxy-2,4,6-trimethyl-non-8-en-3-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: Bu₂BOTf; Et₃N / CH₂Cl₂ / 0 °C

1.2: 49 percent / CH₂Cl₂ / 3 h / -78 - 0 °C

2.1: 63 percent / LiBH₄; H₂O / diethyl ether; tetrahydrofuran / 4 h / 0 - 25 °C

3.1: camphosulfonic acid / CH₂Cl₂ / 1 h / -78 °C

3.2: 55 percent / Dess-Martin periodinane reagent / CH₂Cl₂ / 2 h / 0 - 25 °C

4.1: 62 percent / iPr₂NH; nBuLi / tetrahydrofuran / 0.33 h / -78 °C

With lithium borohydride; n-butyllithium; di-n-butylboryl trifluoromethanesulfonate; camphor-10-sulfonic acid; water; triethylamine; diisopropylamine; In tetrahydrofuran; diethyl ether; dichloromethane; 1.1: addition / 1.2: Condensation / 2.1: Reduction / 3.1: Condensation / 3.2: Oxidation / 4.1: Condensation;
DOI:10.1016/S0040-4020(99)00301-4