<1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

Base Information

Chemical Name:<1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol
CAS No.:106139-90-6
Molecular Formula:C₂₄H₃₀O₆
Molecular Weight:414.499
Hs Code.:

Synonyms:<1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

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Chemical Property of <1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

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Technology Process of <1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

There total 8 articles about <1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)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:

: 119111-14-7
<1S-(1α,2α,3β,4α,5β)>-2-Hydroxy-5-(methoxymethyl)-3,4-bis(phenylmethoxy)cyclopentanemethanol

: 106139-90-6
<1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

Guidance literature:: Multi-step reaction with 3 steps

1: 72 percent / 4-(dimethylamino)pyridine / pyridine / 72 h / Ambient temperature

2: 95 percent / 4-(dimethylamino)pyridine / pyridine / 0 °C

3: CH₃COOH, H₂O / Ambient temperature

With dmap; water; acetic acid; In pyridine;
DOI:10.1021/ja00187a031

Reference yield:

: 106139-74-6
<(2R)-(2α,4aβ,5β,6α,7β,7aβ)>-Hexahydro-5-(methoxymethyl)-2-phenyl-6,7-bis(phenylmethoxy)cyclopenta-1,3-dioxin

: 106139-90-6
<1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

Guidance literature:: Multi-step reaction with 4 steps

1: oxalic acid (aq.) / CH₂Cl₂

2: 72 percent / 4-(dimethylamino)pyridine / pyridine / 72 h / Ambient temperature

3: 95 percent / 4-(dimethylamino)pyridine / pyridine / 0 °C

4: CH₃COOH, H₂O / Ambient temperature

With dmap; water; oxalic acid; acetic acid; In pyridine; dichloromethane;
DOI:10.1021/ja00187a031

Reference yield:

: 119111-15-8
<1R-(1α,2α,3β,4α,5β)>-3-(Methoxymethyl)-4,5-bis(phenylmethoxy)-2-<(triphenylmethoxy)methyl>cyclopentanol

: 106139-90-6
<1R-(1α,2α,3β,4α,5β)>-2-(Acetoxymethyl)-3-(methoxymethyl)-4,5-bis(phenylmethoxy)cyclopentanol

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / 4-(dimethylamino)pyridine / pyridine / 0 °C

2: CH₃COOH, H₂O / Ambient temperature

With dmap; water; acetic acid; In pyridine;
DOI:10.1021/ja00187a031