1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

Base Information

Chemical Name:1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester
CAS No.:220453-33-8
Molecular Formula:C₂₁H₂₄F₃NO₃
Molecular Weight:395.422
Hs Code.:

1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3a<i>H</i>-oxazolo[3,2-<i>a</i>]quinoline-7-carboxylic acid ethyl ester

Synonyms:1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

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Chemical Property of 1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

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Technology Process of 1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

There total 7 articles about 1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester 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: 68.0%

: 140-88-5,9003-32-1
ethyl acrylate

: 220453-31-6
3-phenyl-8a-trifluoromethyl-5-vinyl-2,3,8,8a-tetrahydro-7H-oxazolo[3,2-a]pyridine

: 220453-33-8
1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

Guidance literature:: DOI:10.1021/ja9925958

Reference yield:

: 220453-11-2
phosphoric acid diphenyl ester 3-phenyl-8a-trifluoromethyl-2,3,8,8a-tetrahydro-7H-oxazolo[3,2-a]pyridin-5-yl ester

: 220453-33-8
1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Pd(PPh₃)4

2: 68 percent

With tetrakis(triphenylphosphine) palladium⁽⁰⁾; 1: Substitution / 2: Cycloaddition;
DOI:10.1021/ja9925958

Reference yield:

: 20989-17-7
(2S)-2-phenylglycinol

: 220453-33-8
1-phenyl-3a-trifluoromethyl-1,2,4,5,6,7,8,9-octahydro-3aH-oxazolo[3,2-a]quinoline-7-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 70 percent / p-toluenesulfonic acid

2: KHMDS, HMPA

3: LiCl, Pd(PPh₃)4 / tetrahydrofuran / 2 h / Heating

4: tetrahydrofuran

5: SiO₂ / 1 h

With N,N,N,N,N,N-hexamethylphosphoric triamide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; silica gel; potassium hexamethylsilazane; toluene-4-sulfonic acid; lithium chloride; In tetrahydrofuran;
DOI:10.1021/ja983389n