2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

Base Information

Chemical Name:2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde
CAS No.:163117-74-6
Molecular Formula:C₃₁H₃₄O₄
Molecular Weight:470.609
Hs Code.:

Synonyms:2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

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Chemical Property of 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

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Technology Process of 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

There total 4 articles about 2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-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: 77.0%

: 150356-72-2
3-carboethoxyphenyltributylstannane

: 163117-73-5
2-trifluoromethylsulphonyloxy-3-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxybenzaldehyde

: 163117-74-6
2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; lithium chloride; In N,N-dimethyl-formamide; at 150 ℃; for 2.75h;
DOI:10.1016/S0968-0896(00)00047-X

Reference yield:

: 24677-78-9
2,3-dihydroxybenzaldehyde

: 163117-74-6
2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride; DMSO / 1 h / 20 °C

1.2: 44 percent / dimethylsulfoxide / 20 °C

2.1: 47 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 0.5 h / 0 °C

3.1: 77 percent / bis(triphenylphosphine)palladium dichloride; LiCl / dimethylformamide / 2.75 h / 150 °C

With dmap; bis-triphenylphosphine-palladium(II) chloride; sodium hydride; dimethyl sulfoxide; lithium chloride; In dichloromethane; N,N-dimethyl-formamide; 1.1: deprotonation / 1.2: Substitution / 2.1: trifluoromethylsulphonylation / 3.1: Condensation;
DOI:10.1016/S0968-0896(00)00047-X

Reference yield:

: 163117-71-3
6-chloromethyl-1,2,3,4-tetrahydro-1,1,4,4-tetramethylnaphthalene

: 163117-74-6
2-(5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methoxy-[1,1'-biphenyl]-3'-carboethoxy-6-carboxaldehyde

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride; DMSO / 1 h / 20 °C

1.2: 44 percent / dimethylsulfoxide / 20 °C

2.1: 47 percent / 4-dimethylaminopyridine / CH₂Cl₂ / 0.5 h / 0 °C

3.1: 77 percent / bis(triphenylphosphine)palladium dichloride; LiCl / dimethylformamide / 2.75 h / 150 °C

With dmap; bis-triphenylphosphine-palladium(II) chloride; sodium hydride; dimethyl sulfoxide; lithium chloride; In dichloromethane; N,N-dimethyl-formamide; 1.1: deprotonation / 1.2: Substitution / 2.1: trifluoromethylsulphonylation / 3.1: Condensation;
DOI:10.1016/S0968-0896(00)00047-X