(R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate

Base Information

Chemical Name:(R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate
CAS No.:1262487-80-8
Molecular Formula:C₃₁H₂₆O₇
Molecular Weight:510.543
Hs Code.:

Synonyms:(R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate

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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 (R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate

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Technology Process of (R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate

There total 2 articles about (R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate 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: 94.0%

: 136778-39-7,144015-82-7,144829-37-8,129578-06-9
(+)-goniofufurone

: 102-92-1,17082-09-6
Cinnamoyl chloride

: 1262487-80-8
(R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate

Guidance literature:: With dmap; In acetonitrile; at 0 - 20 ℃; for 30.5h;
DOI:10.1016/j.ejmech.2014.09.064

Reference yield: 83.0%

: (R)-((2R,3R,4R)-3-(cinnamoyloxy)-4,5-dihydroxy-tetrahydrofuran-2-yl)(phenyl)methyl cinnamate

: 1262487-80-8
(R)-((2R,3S,3aS,6aR)-3-(cinnamoyloxy)-5-oxo-hexahydrofuro[3,2-b]furan-2-yl)(phenyl)methyl cinnamate

Guidance literature:: With cycl-isopropylidene malonate; triethylamine; In N,N-dimethyl-formamide; at 0 - 40 ℃; for 36h;
DOI:10.1016/j.tetasy.2010.10.016