((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

Base Information

Chemical Name:((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone
CAS No.:159571-64-9
Molecular Formula:C₁₇H₂₄O₆
Molecular Weight:324.374
Hs Code.:

Synonyms:((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

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Chemical Property of ((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

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Technology Process of ((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

There total 5 articles about ((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone 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: 94.0%

: 107-30-2
chloromethyl methyl ether

: 159571-63-8
((4R,5S)-5-Hydroxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

: 159571-64-9
((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 17h; Ambient temperature;
DOI:10.1016/S0040-4020(01)80644-X

Reference yield:

: 38197-43-2
2-bromo-3-methylanisole

: 159571-64-9
((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / n-butyllihium / hexane; diethyl ether / 0.75 h / -78 °C

2: 97 percent / pyridine, chromium (VI) oxide / CH₂Cl₂ / 0.75 h / Ambient temperature

3: 94 percent / hydrogen / 20percent Pd/C / methanol / 15 h / 760 Torr / Ambient temperature

4: 94 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 17 h / Ambient temperature

With pyridine; chromium(VI) oxide; n-butyllithium; hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; diethyl ether; hexane; dichloromethane;
DOI:10.1016/S0040-4020(01)80644-X

Reference yield:

: 81028-12-8
(4S,5R)-4-benzyloxymethyl-2,2-dimethyl-1,3-dioxolane-5-carboxaldehyde

: 159571-64-9
((4R,5S)-5-Methoxymethoxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-(2-methoxy-6-methyl-phenyl)-methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / n-butyllihium / hexane; diethyl ether / 0.75 h / -78 °C

2: 97 percent / pyridine, chromium (VI) oxide / CH₂Cl₂ / 0.75 h / Ambient temperature

3: 94 percent / hydrogen / 20percent Pd/C / methanol / 15 h / 760 Torr / Ambient temperature

4: 94 percent / N,N-diisopropylethylamine / CH₂Cl₂ / 17 h / Ambient temperature

With pyridine; chromium(VI) oxide; n-butyllithium; hydrogen; N-ethyl-N,N-diisopropylamine; palladium on activated charcoal; In methanol; diethyl ether; hexane; dichloromethane;
DOI:10.1016/S0040-4020(01)80644-X