(2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

Base Information

Chemical Name:(2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine
CAS No.:119237-83-1
Molecular Formula:C₂₁H₂₄O₃
Molecular Weight:324.42
Hs Code.:

Synonyms:(2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

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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 (2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

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Technology Process of (2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

There total 3 articles about (2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine 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:

: 119111-17-0
(2R,4S,5R)-4-((R)-2-Benzyloxy-but-3-enyl)-2-phenyl-[1,3]dioxan-5-ol

: 119237-83-1
(2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

Guidance literature:: Multi-step reaction with 2 steps

1: CH₂Cl₂ / 2 h / Heating

2: AIBN, Bu₃SnH / toluene / 3 h / Heating

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In dichloromethane; toluene;
DOI:10.1021/ja00187a031

Reference yield:

: 115859-25-1,115859-26-2
3-deoxy-2-O-(phenylmethyl)-4,6-O-(phenylmethylene)-D-ribo-hexopyranose

: 119237-83-1
(2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) n-BuLi / 1.) THF, hexane, -20 deg C --> room temp., 1h, 2.) -20 deg C --> room temp., 16h, 3.) 50 deg C, 15 min

2: CH₂Cl₂ / 2 h / Heating

3: AIBN, Bu₃SnH / toluene / 3 h / Heating

With n-butyllithium; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In dichloromethane; toluene;
DOI:10.1021/ja00187a031

Reference yield:

: Imidazole-1-carbothioic acid O-[(2R,4S,5R)-4-((R)-2-benzyloxy-but-3-enyl)-2-phenyl-[1,3]dioxan-5-yl] ester

: 119237-83-1
(2R,4aS,5S,6R,7aS)-6-Benzyloxy-5-methyl-2-phenyl-hexahydro-cyclopenta[1,3]dioxine

: 119111-18-1
<2R-(2α,4aβ,5β,6α,7aβ)>-Hexahydro-5-methyl-2-phenyl-6-(phenylmethoxy)cyclopenta-1,3-dioxin

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; for 3h; Yield given. Yields of byproduct given. Title compound not separated from byproducts; Heating;
DOI:10.1021/ja00187a031