N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

Base Information

Chemical Name:N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide
CAS No.:375385-78-7
Molecular Formula:C₂₀H₂₀ClNO₂
Molecular Weight:341.837
Hs Code.:

Synonyms:N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

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Chemical Property of N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

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Technology Process of N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

There total 3 articles about N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide 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: 90.0%

: 2787-43-1
(3E)-3-methylpenta-1,3-diene

: 375385-72-1
N-(3-chloro-4,4-dimethoxy-cyclohexa-2,5-dienylidene)-benzamide

: 375385-78-7
N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

Guidance literature:: (3E)-3-methylpenta-1,3-diene; N-(3-chloro-4,4-dimethoxy-cyclohexa-2,5-dienylidene)-benzamide; In dichloromethane; at 50 ℃; for 12h; under 9750780 Torr;

With hydrogenchloride; In tetrahydrofuran; for 0.0833333h;
DOI:10.1139/v03-188

Reference yield:

: N-(3-chloro-4,4-dimethoxy-7,8-dimethyl-4a,5,8,8a-tetrahydro-4H-naphthalen-1-ylidene)-benzamide

: 375385-78-7
N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

Guidance literature:: hydrogenchloride; In tetrahydrofuran; for 0.0833333h;
DOI:10.1021/ol016562k

Reference yield:

: N-(3-chloro-4-methoxy-phenyl)-benzamide

: 375385-78-7
N-(3-chloro-4-methoxy-7,8-dimethyl-5,8-dihydronaphthalen-1-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: 59 percent / LiClO₄ / NaHCO₃ / Electrochemical reaction

2.1: CH₂Cl₂ / 12 h / 50 °C / 9750780 Torr

2.2: 90 percent / aq. HCl / tetrahydrofuran / 0.08 h

With lithium perchlorate; sodium hydrogencarbonate; In dichloromethane; 2.1: Diels-Alder reaction;
DOI:10.1139/v03-188