(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

Base Information

Chemical Name:(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde
CAS No.:260371-65-1
Molecular Formula:C₂₄H₂₅NO₄
Molecular Weight:391.467
Hs Code.:

Synonyms:(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

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Chemical Property of (S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

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Technology Process of (S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

There total 5 articles about (S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde 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: 57.0%

: 2550-36-9
Cyclohexylmethyl bromide

: 260371-64-0
(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]salicylaldehyde

: 260371-65-1
(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

Guidance literature:: (S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]salicylaldehyde; With caesium carbonate; In methanol; water; at 20 ℃; for 0.5h;

Cyclohexylmethyl bromide; In N,N-dimethyl-formamide; at 90 ℃; for 2h;
DOI:10.1016/S0957-4166(99)00470-X

Reference yield:

: 85-44-9
phthalic anhydride

: 260371-65-1
(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1.1: 65 percent / CHCl₃ / 96 h / Heating

2.1: 90 percent / TiCl₄ / CH₂Cl₂ / 1.25 h / 0 °C

3.1: 99 percent / BCl₃ / CH₂Cl₂ / 24 h / 20 °C

4.1: Cs₂CO₃ / methanol; H₂O / 0.5 h / 20 °C

4.2: 57 percent / dimethylformamide / 2 h / 90 °C

With boron trichloride; titanium tetrachloride; caesium carbonate; In methanol; dichloromethane; chloroform; water; 1.1: Acylation / 2.1: Formylation / 3.1: demethylation / 4.1: Metallation / 4.2: Alkylation;
DOI:10.1016/S0957-4166(99)00470-X

Reference yield:

: 6298-96-0,22038-86-4,35600-82-9,41851-59-6
(S)-1-(4-methoxyphenyl)ethylamine

: 260371-65-1
(S)-5-[1-(1,3-dioxoisoindolin-2-yl)ethyl]-2-(cyclohexylmethoxy)benzaldehyde

Guidance literature:: Multi-step reaction with 4 steps

1.1: 65 percent / CHCl₃ / 96 h / Heating

2.1: 90 percent / TiCl₄ / CH₂Cl₂ / 1.25 h / 0 °C

3.1: 99 percent / BCl₃ / CH₂Cl₂ / 24 h / 20 °C

4.1: Cs₂CO₃ / methanol; H₂O / 0.5 h / 20 °C

4.2: 57 percent / dimethylformamide / 2 h / 90 °C

With boron trichloride; titanium tetrachloride; caesium carbonate; In methanol; dichloromethane; chloroform; water; 1.1: Acylation / 2.1: Formylation / 3.1: demethylation / 4.1: Metallation / 4.2: Alkylation;
DOI:10.1016/S0957-4166(99)00470-X