(-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

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Chemical Name:(-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one
CAS No.:736140-50-4
Molecular Formula:C₂₄H₂₇NO₅
Molecular Weight:409.482
Hs Code.:

Synonyms:(-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

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Chemical Property of (-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

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Technology Process of (-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

There total 2 articles about (-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-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: 97.0%

: 736140-49-1
(+)-4S-ethenyl-5S-[2-(4-methoxyphenyl)methoxy]ethyl-3-(1S-phenylmethoxymethyl-2-propenyl)-1,3-oxazolidin-2-one

: 736140-50-4
(-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

Guidance literature:: Grubbs catalyst first generation; In dichloromethane; for 42h; Heating;
DOI:10.1016/j.tet.2004.05.010

Reference yield:

: 736140-48-0
(+)-1-(4-methoxyphenyl)methoxy-(4S)-[(1S-phenylmethoxymethyl)-2-propenylamino]-5-hexen-3S-ol

: 736140-50-4
(-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / Et₃N / CH₂Cl₂ / 2.5 h / 0 °C

2: 97 percent / benzylidenebis(tricyclohexylphosphine)ruthenium dichloride / CH₂Cl₂ / 42 h / Heating

With triethylamine; Grubbs catalyst first generation; In dichloromethane;
DOI:10.1016/j.tet.2004.05.010

Reference yield: 85.0%

: 736140-50-4
(-)-(1S,5S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,7a-dihydro-1H,3H-pyrrolo[1,2-c]oxazol-3-one

: 736140-51-5
(-)-(1S,5S,6R,7S,7aS)-1-[2-(4-methoxyphenyl)methoxy]ethyl-5-(phenylmethoxy)methyl-5,6,7,7a-tetrahydro-6,7-dihydroxy-1H,3H-pyrrolo[1,2-c]oxazol-3-one

Guidance literature:: With potassium osmate(VI); 4-methylmorpholine N-oxide; In water; acetone; at 20 ℃; for 21h;
DOI:10.1016/j.tet.2004.05.010