(3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one

Base Information

Chemical Name:(3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one
CAS No.:1020737-59-0
Molecular Formula:C₂₀H₂₉NO₃
Molecular Weight:331.455
Hs Code.:

Synonyms:(3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one

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Chemical Property of (3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one

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Technology Process of (3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one

There total 1 articles about (3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-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: 82.0%

: 52331-62-1
(E)-3-cyclohexylacryloyl chloride

: 159849-26-0
(1S,2R,6S,7R,exo)-3-oxa-5-aza-7,10,10-trimethyltricyclo<5.2.1.0^2,6>decan-4-one

: 1020737-59-0
(3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one

Guidance literature:: With 18-crown-6 ether; sodium hydride; In tetrahydrofuran; at 20 ℃;
DOI:10.1021/jo800145x

Reference yield:

: 1020737-59-0
(3aS,4R,7S,7aR)-3-[(2E)-3-cyclohexylprop-2-enoyl]-4,8,8-trimethylhexahydro-4,7-methano-1,3-benzoxazol-2(3H)-one

: 1020738-68-4
C₂₀H₃₁NO₅

: 1020738-66-2
C₂₀H₃₁NO₅

Guidance literature:: With ruthenium trichloride; sodium periodate; cerium(III) chloride; In water; acetonitrile; at 0 ℃;
DOI:10.1021/jo800145x