[(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

Base Information

Chemical Name:[(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester
CAS No.:205868-43-5
Molecular Formula:C₂₄H₂₇NO₇
Molecular Weight:441.481
Hs Code.:

Synonyms:[(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

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Chemical Property of [(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

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Technology Process of [(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

There total 11 articles about [(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester 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: 78.0%

: 205868-42-4
{(2R,4R,5S,6R)-4-[(2,5-Dimethoxy-phenyl)-hydroxy-methyl]-2-phenyl-6-vinyl-[1,3]dioxan-5-yl}-methyl-carbamic acid methyl ester

: 205868-43-5
[(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

Guidance literature:: With dipyridinium dichromate; acetic anhydride; In dichloromethane; for 3h; Ambient temperature;
DOI:10.1080/07328309808002322

Reference yield:

: 1125-88-8
benzaldehyde dimethyl acetal

: 205868-43-5
[(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 94 percent / p-TsOH / CH₂Cl₂ / 14 h / Ambient temperature

2: 96 percent / I₂, aq. NaHCO₃ / acetone / 6 h / Ambient temperature

3: 41 percent / n-BuLi / tetrahydrofuran / -60 - 20 °C

4: 78 percent / PDC, Ac₂O / CH₂Cl₂ / 3 h / Ambient temperature

With dipyridinium dichromate; n-butyllithium; iodine; acetic anhydride; sodium hydrogencarbonate; toluene-4-sulfonic acid; In tetrahydrofuran; dichloromethane; acetone;
DOI:10.1080/07328309808002322

Reference yield:

: 25245-34-5
1-bromo-2,5-dimethoxybenzene

: 205868-43-5
[(4R)-(2,5-dimethoxybenzoyl)-(2R)-phenyl-(6R)-vinyl-[1,3]dioxane-(5S)-yl]methylcarbamic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 41 percent / n-BuLi / tetrahydrofuran / -60 - 20 °C

2: 78 percent / PDC, Ac₂O / CH₂Cl₂ / 3 h / Ambient temperature

With dipyridinium dichromate; n-butyllithium; acetic anhydride; In tetrahydrofuran; dichloromethane;
DOI:10.1080/07328309808002322