methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

Base Information

Chemical Name:methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate
CAS No.:467252-56-8
Molecular Formula:C₂₀H₃₂O₈
Molecular Weight:400.469
Hs Code.:

Synonyms:methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

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Chemical Property of methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

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Technology Process of methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

There total 1 articles about methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate 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: 97.0%

: 55289-05-9
methyl 3-hydroxy-2-methylbenzoate

: 130955-38-3
2,5,8,11,14-pentaoxahexadecan-16-yl methanesulfonate

: 467252-56-8
methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

Guidance literature:: With potassium carbonate; In acetonitrile; Heating;
DOI:10.1021/jm0208673

Reference yield: 49.0%

: 467252-56-8
methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

: 467252-58-0
3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzyl alcohol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; for 2h; Heating;
DOI:10.1021/jm0208673

Reference yield:

: 467252-56-8
methyl 3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzoate

: 467252-60-4
3-[2-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethoxy)ethoxy]-2-methylbenzyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: 49 percent / LiAlH₄ / tetrahydrofuran / 2 h / Heating

2: SOCl₂ / CH₂Cl₂ / 0.5 h / 20 °C

With lithium aluminium tetrahydride; thionyl chloride; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm0208673