(2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

Base Information

Chemical Name:(2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane
CAS No.:128461-51-8
Molecular Formula:C₁₉H₂₅IO₃
Molecular Weight:428.31
Hs Code.:

Synonyms:(2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

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Chemical Property of (2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

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Technology Process of (2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

There total 7 articles about (2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane 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:

: 128461-65-4
3-(p-methoxybenzyloxy)propanal

: 128461-51-8
(2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) (c-C₅H₉)2OTf, i-Pr₂NEt / 2.) CH₂Cl₂, -78 deg C

2: 92 percent / DDQ / CH₂Cl₂

3: 1.) LiOH, H₂O₂; 2.) LiAlH₄ / 1.) THF, H₂O; 2.) THF, 0 deg C

4: (ClCO)2, Et₃N / dimethylsulfoxide; CH₂Cl₂ / -78 °C

5: tetrahydrofuran

With lithium hydroxide; lithium aluminium tetrahydride; oxalyl dichloride; (c-C₅H₉)2OTf; dihydrogen peroxide; triethylamine; N-ethyl-N,N-diisopropylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/S0040-4039(00)70631-9

Reference yield:

: 96930-18-6,128461-58-5
(4S,5R)-4-Methyl-3-pent-4-enoyl-5-phenyl-oxazolidin-2-one

: 128461-51-8
(2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) (c-C₅H₉)2OTf, i-Pr₂NEt / 2.) CH₂Cl₂, -78 deg C

2: 92 percent / DDQ / CH₂Cl₂

3: 1.) LiOH, H₂O₂; 2.) LiAlH₄ / 1.) THF, H₂O; 2.) THF, 0 deg C

4: (ClCO)2, Et₃N / dimethylsulfoxide; CH₂Cl₂ / -78 °C

5: tetrahydrofuran

With lithium hydroxide; lithium aluminium tetrahydride; oxalyl dichloride; (c-C₅H₉)2OTf; dihydrogen peroxide; triethylamine; N-ethyl-N,N-diisopropylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/S0040-4039(00)70631-9

Reference yield:

: 128461-59-6
(4R,5S)-3-{(R)-2-[(S)-1-Hydroxy-3-(4-methoxy-benzyloxy)-propyl]-pent-4-enoyl}-4-methyl-5-phenyl-oxazolidin-2-one

: 128461-51-8
(2R,4S)-4-((E)-(R)-1-Allyl-4-iodo-3-methyl-but-2-enyl)-2-(4-methoxy-phenyl)-[1,3]dioxane

Guidance literature:: Multi-step reaction with 5 steps

1: 92 percent / DDQ / CH₂Cl₂

2: 1.) LiOH, H₂O₂; 2.) LiAlH₄ / 1.) THF, H₂O; 2.) THF, 0 deg C

3: (ClCO)2, Et₃N / dimethylsulfoxide; CH₂Cl₂ / -78 °C

4: tetrahydrofuran

With lithium hydroxide; lithium aluminium tetrahydride; oxalyl dichloride; dihydrogen peroxide; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In tetrahydrofuran; dichloromethane; dimethyl sulfoxide;
DOI:10.1016/S0040-4039(00)70631-9