4-[2-[(1R)-1,2,3,4,4a,7,8,8aα-Octahydro-4β-hydroxy-1,2α,4aα,5-tetramethylnaphthalen-1α-yl]ethyl]furan-2(5H)-one

Base Information

Chemical Name:4-[2-[(1R)-1,2,3,4,4a,7,8,8aα-Octahydro-4β-hydroxy-1,2α,4aα,5-tetramethylnaphthalen-1α-yl]ethyl]furan-2(5H)-one
CAS No.:24399-41-5
Molecular Formula:C20H30 O3
Molecular Weight:318.45
Hs Code.:
Mol file:24399-41-5.mol

Synonyms:17,19-Dinor-8bH-labda-3,13-dien-15-oic acid, 6b,16-dihydroxy-5,9-dimethyl-, g-lactone (8CI); 2(5H)-Furanone,4-[2-(1,2,3,4,4a,7,8,8a-octahydro-4-hydroxy-1,2,4a,5-tetramethyl-1-naphthalenyl)ethyl]-,[1R-(1a,2a,4b,4aa,8aa)]-; Elongatolide A; Solidagolactone IV

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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 4-[2-[(1R)-1,2,3,4,4a,7,8,8aα-Octahydro-4β-hydroxy-1,2α,4aα,5-tetramethylnaphthalen-1α-yl]ethyl]furan-2(5H)-one

Chemical Property:

PSA：46.53000
LogP:4.01940

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 4-[2-[(1R)-1,2,3,4,4a,7,8,8aα-Octahydro-4β-hydroxy-1,2α,4aα,5-tetramethylnaphthalen-1α-yl]ethyl]furan-2(5H)-one

There total 4 articles about 4-[2-[(1R)-1,2,3,4,4a,7,8,8aα-Octahydro-4β-hydroxy-1,2α,4aα,5-tetramethylnaphthalen-1α-yl]ethyl]furan-2(5H)-one 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: 90.0%

: 41943-77-5
Solidagolacton V

: 24399-41-5,106190-17-4
Solidagolacton IV

Guidance literature:: With sodium tetrahydroborate; In methanol; at -84 ℃; for 3h; Reagent/catalyst; stereoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2016.09.062

Reference yield: 14.0%

: 41943-77-5
Solidagolacton V

: 24399-41-5,106190-17-4
Solidagolacton IV

: C₂₀H₃₀O₃

Guidance literature:: With sodium tetrahydroborate; yttrebium(III) chloride hydrate; In methanol; at -84 ℃; for 3h; Overall yield = 100 %; stereoselective reaction;
DOI:10.1016/j.tet.2016.09.062