Hexanoic acid, 4-[(2-methoxyethoxy)methoxy]-5-oxo-6-(phenylmethoxy)-

Base Information

Chemical Name:Hexanoic acid, 4-[(2-methoxyethoxy)methoxy]-5-oxo-6-(phenylmethoxy)-
CAS No.:737799-86-9
Molecular Formula:C17H24O7
Molecular Weight:340.373
Hs Code.:
DSSTox Substance ID:DTXSID20463557
Nikkaji Number:J2.061.814K

Synonyms:737799-86-9;Hexanoic acid, 4-[(2-methoxyethoxy)methoxy]-5-oxo-6-(phenylmethoxy)-;DTXSID20463557

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Hexanoic acid, 4-[(2-methoxyethoxy)methoxy]-5-oxo-6-(phenylmethoxy)-

Chemical Property:

XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:14
Exact Mass:340.15220310
Heavy Atom Count:24
Complexity:353

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:COCCOCOC(CCC(=O)O)C(=O)COCC1=CC=CC=C1

Technology Process of Hexanoic acid, 4-[(2-methoxyethoxy)methoxy]-5-oxo-6-(phenylmethoxy)-

There total 2 articles about Hexanoic acid, 4-[(2-methoxyethoxy)methoxy]-5-oxo-6-(phenylmethoxy)- 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: 40.0%

: 737799-85-8
2-benzyloxymethyl-2-methoxy-3-(2-methoxy-ethoxymethoxy)-tetrahydro-pyran

: 737799-86-9
6-(benzyloxy)-4-[(2-methoxyethoxy)methoxy]-5-oxohexanoic acid

Guidance literature:: With jones reagent; In acetone; at 20 ℃; for 5h;
DOI:10.1016/j.tetlet.2004.05.089

Reference yield:

: 89429-82-3
6-benzyloxymethyl-3,4-dihydro-2H-pyran

: 737799-86-9
6-(benzyloxy)-4-[(2-methoxyethoxy)methoxy]-5-oxohexanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1.1: n-CPBA / 2 h / 0 °C

1.2: 77 percent / DIPEA / 20 h / 20 °C

2.1: 40 percent / Jones reagent / acetone / 5 h / 20 °C

With jones reagent; In acetone; 2.1: Jones oxidation;
DOI:10.1016/j.tetlet.2004.05.089