5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

Base Information

Chemical Name:5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate
CAS No.:781658-89-7
Molecular Formula:C₂₂H₂₆O₆
Molecular Weight:386.445
Hs Code.:

Synonyms:5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

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Chemical Property of 5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

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Technology Process of 5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

There total 1 articles about 5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate 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: 86.7%

: 108-24-7
acetic anhydride

: 5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methyl]oxolan-2-ol

: 781658-89-7
5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

Guidance literature:: With pyridine; at 20 ℃; for 72h;
DOI:10.1021/jm049550o

Reference yield: 100.0%

: 64339-87-3
N₄,O-bis(trimethylsilyl)-N₄-benzoylcytosine

: 781658-89-7
5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

: 781658-90-0
N-(1-{5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methyl]oxolan-2-yl}-2-oxohydropyrimidin-4-yl)benzamide

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In 1,2-dichloro-ethane; at 20 ℃; for 20h;
DOI:10.1021/jm049550o

Reference yield:

: 781658-89-7
5-[(4-methoxyphenoxy)methyl]-5-[(phenylmethoxy)methy-l]oxolan-2-yl acetate

: 4-Amino-1-[(2S,5R)-5-ethynyl-5-(4-methoxy-phenoxymethyl)-tetrahydro-furan-2-yl]-1H-pyrimidin-2-one

Guidance literature:: Multi-step reaction with 5 steps

1.1: 100 percent / trimethylsilyl trifluoromethanesulfonate / 1,2-dichloro-ethane / 20 h / 20 °C

2.1: 1.43 g / BCl₃ / CH₂Cl₂ / 3 h / -78 °C

3.1: 1,3-dicyclohexylcarbodiimide; dichloroacetic acid; DMSO / 1.5 h / 0 °C

4.1: n-BuLi / tetrahydrofuran; hexane / 1 h / -78 °C

4.2: tetrahydrofuran; hexane / 3 h / -78 - 0 °C

5.1: n-BuLi / tetrahydrofuran; hexane / 2 h / -78 °C

With dichloro-acetic acid; n-butyllithium; trimethylsilyl trifluoromethanesulfonate; boron trichloride; dimethyl sulfoxide; dicyclohexyl-carbodiimide; In tetrahydrofuran; hexane; dichloromethane; 1,2-dichloro-ethane; 4.2: Wittig olefination;
DOI:10.1021/jm049550o