<1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

Base Information

Chemical Name:<1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol
CAS No.:115859-29-5
Molecular Formula:C₂₂H₂₈O₄
Molecular Weight:356.462
Hs Code.:

Synonyms:<1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

Suppliers and Price of <1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

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 <1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of <1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

There total 3 articles about <1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol 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: 65.0%

: 106139-77-9
<(2R)-(2α,4aβ,5β,6α,7aβ)>-hexahydro-5-(methoxymethyl)-2-phenyl-6-(phenylmethoxy)cyclopenta-1,3-dioxin

: 115859-29-5
<1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

: 115859-30-8
<1S-(1α,2β,3α,5α)>-2-(methoxymethyl)-3,5-bis(phenylmethoxy)cyclopentanemethanol

Guidance literature:: With lithium aluminium tetrahydride; aluminium trichloride; In diethyl ether; dichloromethane; for 1h; Ambient temperature;
DOI:10.1021/jo00254a020

Reference yield:

: 115859-28-4,116002-03-0
Imidazole-1-carbothioic acid O-[(2R,4S,5R)-4-((Z)-(R)-2-benzyloxy-4-methoxy-but-3-enyl)-2-phenyl-[1,3]dioxan-5-yl] ester

: 115859-29-5
<1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

Guidance literature:: Multi-step reaction with 2 steps

1: Bu₃SnH, AIBN / toluene / 2 h / Heating

2: 19 percent / LAH, AlCl₃ / CH₂Cl₂; diethyl ether / 1 h / Ambient temperature

With lithium aluminium tetrahydride; aluminium trichloride; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In diethyl ether; dichloromethane; toluene;
DOI:10.1021/jo00254a020

Reference yield:

: 115859-27-3,115938-45-9
2,4-dideoxy-1-O-methyl-3-(phenylmethyl)-5,7-O-(phenylmethylene)-D-ribo-hept-1-enitol

: 115859-29-5
<1S-(1α,2α,3β,4α)>-3-(methoxymethyl)-4-(phenylmethoxy)-2-<(phenylmethoxy)methyl>cyclopentanol

Guidance literature:: Multi-step reaction with 3 steps

1: 74 percent / 1,2-dichloro-ethane / 3 h / Heating

2: Bu₃SnH, AIBN / toluene / 2 h / Heating

3: 19 percent / LAH, AlCl₃ / CH₂Cl₂; diethyl ether / 1 h / Ambient temperature

With lithium aluminium tetrahydride; aluminium trichloride; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In diethyl ether; dichloromethane; 1,2-dichloro-ethane; toluene;
DOI:10.1021/jo00254a020