<3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

Base Information

Chemical Name:<3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester
CAS No.:101469-46-9
Molecular Formula:C₁₆H₁₆O₆
Molecular Weight:304.299
Hs Code.:

<3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopenta<c>furan-4-carbonsaeure-methylester

Synonyms:

Suppliers and Price of <3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

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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 <3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

Chemical Property:

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Technology Process of <3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

There total 1 articles about <3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester 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:

: 98-88-4
benzoyl chloride

: 88511-03-9
(3aS-cis)-3,3a,6,6a-Tetrahydro-5-hydroxy-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

: 101469-46-9
<3aS-(3aα,4β,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

: 101375-86-4
<3aS-(3aα,4α,5β,6aα)>-Hexahydro-5-(benzoyloxy)-1-oxo-1H-cyclopentafuran-4-carbonsaeure-methylester

Guidance literature:: With hydrogen; platinum(IV) oxide; Yield given. Multistep reaction. Yields of byproduct given; 1.) methyl acetate, 25 deg C, 760 Torr, 1h 2.) pyridine, 0 deg C, 14h;
DOI:10.1002/jlac.198619860706