2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

Base Information

Chemical Name:2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one
CAS No.:946570-46-3
Molecular Formula:C₂₄H₂₈O₆
Molecular Weight:412.483
Hs Code.:

Synonyms:2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

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Chemical Property of 2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

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Technology Process of 2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

There total 7 articles about 2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-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: 15.0%

: C₂₄H₃₀O₇

: 946570-46-3
2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

Guidance literature:: C₂₄H₃₀O₇; With methanesulfonyl chloride; triethylamine; In dichloromethane; at 0 - 20 ℃; for 3h;

With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 20 ℃; Further stages.;
DOI:10.1021/jm0702579

Reference yield:

: 946570-44-1
4-methoxy-1-({4-methylene-2-[(phenylmethoxy)methyl](1,3-dioxolan-2-yl)}methoxy)benzene

: 946570-46-3
2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: O₃ / CH₂Cl₂; methanol / -78 °C

1.2: 71 percent / dimethyl sulfide / CH₂Cl₂; methanol / 2 h / 20 °C

2.1: lithium diisopropylamide / tetrahydrofuran; hexane / 0.5 h / -78 °C

2.2: tetrahydrofuran; hexane / 2 h / -78 °C

3.1: Et₃N; methanesulfonyl chloride / CH₂Cl₂ / 3 h / 0 - 20 °C

3.2: 15 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 20 °C

With ozone; methanesulfonyl chloride; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane;
DOI:10.1021/jm0702579

Reference yield:

: 946570-43-0
1-({4-(chloromethyl)-2-[(phenylmethoxy)methyl](1,3-dioxolan-2-yl)}methoxy)-4-methoxybenzene

: 946570-46-3
2-[(4-methoxyphenoxy)methyl]-5-(3-methylbutylidene)-2-[(phenylmethoxy)methyl]-1,3-dioxolan-4-one

Guidance literature:: Multi-step reaction with 4 steps

1.1: 80 percent / tBuOK / tetrahydrofuran / 19 h / Heating

2.1: O₃ / CH₂Cl₂; methanol / -78 °C

2.2: 71 percent / dimethyl sulfide / CH₂Cl₂; methanol / 2 h / 20 °C

3.1: lithium diisopropylamide / tetrahydrofuran; hexane / 0.5 h / -78 °C

3.2: tetrahydrofuran; hexane / 2 h / -78 °C

4.1: Et₃N; methanesulfonyl chloride / CH₂Cl₂ / 3 h / 0 - 20 °C

4.2: 15 percent / 1,8-diazabicyclo[5.4.0]undec-7-ene / CH₂Cl₂ / 20 °C

With potassium tert-butylate; ozone; methanesulfonyl chloride; triethylamine; lithium diisopropyl amide; In tetrahydrofuran; methanol; hexane; dichloromethane;
DOI:10.1021/jm0702579