(8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:(8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester
CAS No.:951330-73-7
Molecular Formula:C₁₈H₂₂FNO₃
Molecular Weight:319.376
Hs Code.:

Synonyms:(8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

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Chemical Property of (8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

Chemical Property:

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Technology Process of (8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

There total 1 articles about (8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl 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: 26.7%

: 188975-88-4
tert-butyl 4-oxoazepane-1-carboxylate

: 459-57-4
4-fluorobenzaldehyde

: 951330-73-7
(8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: tert-butyl 4-oxoazepane-1-carboxylate; With morpholine; toluene-4-sulfonic acid; In water; benzene; for 2h; Heating / reflux;

4-fluorobenzaldehyde; In water; benzene; Heating / reflux;

Reference yield:

: 951330-73-7
(8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

: 95-92-1
oxalic acid diethyl ester

: 951330-74-8
(8E)-5-ethoxyoxalyl-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

Guidance literature:: (8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃; for 1h;

oxalic acid diethyl ester; In tetrahydrofuran; at -78 - 20 ℃;

With hydrogenchloride; In tetrahydrofuran; water; ethyl acetate;

Reference yield:

: 951330-73-7
(8E)-3-(4-fluoro-benzylidene)-4-oxo-azepane-1-carboxylic acid tert-butyl ester

: (8E)-1-(2,4-dichloro-phenyl)-8-(4-fluoro-benzylidene)-1,4,5,6,7,8-hexahydro-1,2,6-triaza-azulene-3-carboxylic acid piperidin-1-ylamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -78 °C

1.2: -78 - 20 °C

2.1: ethanol / 20 °C

3.1: lithium hydroxide; water / tetrahydrofuran; ethanol / 20 °C

3.2: pH 4

4.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dmap / N,N-dimethyl-formamide / 20 °C

5.1: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With lithium hydroxide; water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; lithium hexamethyldisilazane; dmap; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;