(2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate

Base Information

Chemical Name:(2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate
CAS No.:228122-03-0
Molecular Formula:C₃₄H₄₂O₇
Molecular Weight:562.703
Hs Code.:

Synonyms:(2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate

Suppliers and Price of (2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate

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 (2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate

There total 2 articles about (2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate 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:

: 217819-76-6
(2S,3R)-2-(benzyloxy)-3-<(p-methoxybenzyl)oxy>-2-<<(p-methoxybenzyl)oxy>methyl>-4-pentenal

: 228122-03-0
(2S,3R)-2-(benzyloxy)-3-[(p-methoxybenzyl)oxy]-2-{[(p-methoxybenzyl)oxy]methyl}-4-penten-1-yl pivalate

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄ / diethyl ether / 0.5 h

2: 4-(dimethylamino)pyridine / CH₂Cl₂ / 5 h

With dmap; lithium aluminium tetrahydride; In diethyl ether; dichloromethane; 1: Reduction / 2: Acylation;
DOI:10.1002/1099-0690(200006)2000:12<2187::AID-EJOC2187<3.0.CO;2-2