4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

Base Information

Chemical Name:4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde
CAS No.:141667-35-8
Molecular Formula:C₁₆H₁₇NO₅S
Molecular Weight:335.381
Hs Code.:

Synonyms:4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

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Chemical Property of 4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

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Technology Process of 4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

There total 3 articles about 4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde 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: 69.0%

: 141667-29-0
3-Methoxy-1-(toluene-4-sulfonyl)-1H-pyridin-2-one

: 107-02-8,25068-14-8
acrolein

: 141667-35-8
4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

Guidance literature:: In dichloromethane; at 90 ℃; for 144h;
DOI:10.1021/jo00041a010

Reference yield:

: 20928-63-6
3-methoxy-1H-pyridin-2-one

: 141667-35-8
4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 1) MeLi / 1) THF, Et₂O, 0 deg C, 20 min, 2) THF, Et₂O, 16 h

2: 69 percent / CH₂Cl₂ / 144 h / 90 °C

With methyllithium; In dichloromethane;
DOI:10.1021/jo00041a010

Reference yield:

: 98-59-9
p-toluenesulfonyl chloride

: 141667-35-8
4-methoxy-2-(4'-methylbenzenesulfonyl)-3-oxo-2-azabicyclo<2.2.2>oct-7-ene-5-endo-carboxaldehyde

Guidance literature:: Multi-step reaction with 2 steps

1: 1) MeLi / 1) THF, Et₂O, 0 deg C, 20 min, 2) THF, Et₂O, 16 h

2: 69 percent / CH₂Cl₂ / 144 h / 90 °C

With methyllithium; In dichloromethane;
DOI:10.1021/jo00041a010