1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Base Information

Chemical Name:1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane
CAS No.:121404-89-5
Molecular Formula:C₃₁H₃₂O₆
Molecular Weight:500.591
Hs Code.:

Synonyms:1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Suppliers and Price of 1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

There total 29 articles about 1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane 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:

: 121404-84-0
4-iodo-3-(2-iodo-5-methoxybenzoyloxy)benzaldehyde

: 121404-89-5
1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Guidance literature:: Multi-step reaction with 4 steps

1: 20 percent / Ni(O)(Ph₃P)4

4: LiAlH₄ / tetrahydrofuran

With lithium aluminium tetrahydride; Ni(O)(Ph₃P)4; In tetrahydrofuran;
DOI:10.1016/S0040-4039(00)80674-7

Reference yield:

: 121404-87-3
4-{2-Methoxy-5-[(E)-2-(8-methoxy-6-oxo-6H-benzo[c]chromen-3-yl)-vinyl]-phenoxy}-benzoic acid methyl ester

: 121404-89-5
1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Guidance literature:: Multi-step reaction with 2 steps

2: LiAlH₄ / tetrahydrofuran

With lithium aluminium tetrahydride; In tetrahydrofuran;
DOI:10.1016/S0040-4039(00)80674-7

Reference yield:

: 621-59-0
isovanillin

: 121404-89-5
1-<4-(2-hydroxymethyl-4-methoxyphenyl)-3-methoxyphenyl>-2-<3-(4-hydroxymethylphenoxy)-4-methoxyphenyl>ethane

Guidance literature:: Multi-step reaction with 8 steps

1: 96 percent / NH₄NO₃ / ethanol / 24 h

2: 30 percent / K₂CO₃, CuO / pyridine / 48 h / Heating

3: 90 percent / NaBH₄ / ethanol / 1 h

4: 47percent HBr / benzene; H₂O / 1 h

5: 76 percent / acetonitrile / 1 h / Heating

6: 1) NaOMe, 2) H₂ / Pd-charcoal / 1) methylene dichloride, methanol, 1h, 2) methanol, ethyl acetate

7: LiAlH₄ / tetrahydrofuran

8: 30 percent / CH₂Cl₂; diethyl ether / 5 h

With ammonium nitrate; sodium tetrahydroborate; lithium aluminium tetrahydride; hydrogen bromide; hydrogen; sodium methylate; potassium carbonate; copper(II) oxide; palladium on activated charcoal; In tetrahydrofuran; pyridine; diethyl ether; ethanol; dichloromethane; water; acetonitrile; benzene;