1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene

Base Information

Chemical Name:1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene
CAS No.:1245616-46-9
Molecular Formula:C₂₀H₂₈O₃
Molecular Weight:316.441
Hs Code.:

Synonyms:1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene

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Technology Process of 1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene

There total 1 articles about 1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene 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: 84.0%

: 1245616-67-4
(1S,2S)-1-(3,3-dimethylcycloprop-1-enyl)-3-(4-methoxybenzyloxy)-2-methylpropan-1-ol

: 106-95-6
allyl bromide

: 1245616-46-9
1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene

Guidance literature:: With potassium tert-butylate; In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1021/ol101741f

Reference yield: 93.0%

: 1245616-46-9
1-[(2S,3S)-3-allyloxy-3-(3,3-dimethylcycloprop-1-enyl)-2-methyl-propoxymethyl]-4-methoxybenzene

: 1245616-57-2
(1S,4S,6R)-5-isopropylidene-4-[(S)-2-(4-methoxybenzyloxy)-1-methylethyl]-3-oxabicyclo-[4.1.0]heptane

Guidance literature:: With gold(I) chloride; In dichloromethane; at 0 ℃; for 0.25h; optical yield given as %de; diastereoselective reaction;
DOI:10.1021/ol101741f