(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

Base Information

Chemical Name:(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one
CAS No.:86970-91-4
Molecular Formula:C₁₉H₁₉NO₄
Molecular Weight:325.364
Hs Code.:

Synonyms:(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

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Chemical Property of (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

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Technology Process of (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

There total 6 articles about (1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-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:

: N-(3,4-dimethoxyphenethyl)-5-phenyloxazolidin-2-one

: 86970-91-4
(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

: (1R,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

Guidance literature:: With toluene-4-sulfonic acid; In acetonitrile; at 100 ℃; for 3h; under 2585.81 Torr; Overall yield = 75 %; Overall yield = 12.2 mg; Microwave irradiation;
DOI:10.3987/COM-18-S(F)21

Reference yield:

: 5841-63-4
5-phenyloxazolidine-2,4-dione

: 86970-91-4
(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / triphenylphosphine, diisopropyl azodicarboxylate / tetrahydrofuran / 14 h / Ambient temperature

2: 1.) (i-Bu)2AlH, 2.) HCOOH / 1.) toluene, -78 deg C, 1 h, 2.) room temp., 14 h

With formic acid; di-isopropyl azodicarboxylate; diisobutylaluminium hydride; triphenylphosphine; In tetrahydrofuran;
DOI:10.1021/jo00169a054

Reference yield:

: 7417-21-2
2-(3,4-dimethoxyphenyl)ethyl alcohol

: 86970-91-4
(1S,10bS)-8,9-Dimethoxy-1-phenyl-1,5,6,10b-tetrahydro-oxazolo[4,3-a]isoquinolin-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / triphenylphosphine, diisopropyl azodicarboxylate / tetrahydrofuran / 14 h / Ambient temperature

2: 1.) (i-Bu)2AlH, 2.) HCOOH / 1.) toluene, -78 deg C, 1 h, 2.) room temp., 14 h

With formic acid; di-isopropyl azodicarboxylate; diisobutylaluminium hydride; triphenylphosphine; In tetrahydrofuran;
DOI:10.1021/jo00169a054