3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

Base Information

Chemical Name:3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
CAS No.:1269636-28-3
Molecular Formula:C₂₇H₁₇BCl₂F₂N₂
Molecular Weight:489.159
Hs Code.:

Synonyms:3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

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Chemical Property of 3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

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Technology Process of 3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

There total 4 articles about 3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene 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: 46.0%

: 37629-37-1,21461-46-1
2-(2-nitrovinyl)naphthalene

: 1269636-16-9
8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

: 1269636-28-3
3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

Guidance literature:: With 18-crown-6 ether; potassium carbonate; thiophenol; In N,N-dimethyl-formamide; at 20 ℃; Inert atmosphere;
DOI:10.1021/ol200148u

Reference yield:

: 83-38-5
2,6-dichlorobenzaldehyde

: 1269636-28-3
3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride; water / 6 h / 20 °C / Inert atmosphere

2: chloranil / dichloromethane / Inert atmosphere

3: boron trifluoride diethyl etherate; triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

4: 18-crown-6 ether; potassium carbonate; thiophenol / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

With hydrogenchloride; 18-crown-6 ether; boron trifluoride diethyl etherate; water; chloranil; potassium carbonate; thiophenol; triethylamine; In dichloromethane; N,N-dimethyl-formamide; 4: Michel-addition/Vicarious Nucleophilic Substitution styrylation;
DOI:10.1021/ol200148u

Reference yield:

: 1165898-88-3
5-(2,6-Dichlorophenyl)dipyrromethene

: 1269636-28-3
3-(2-naphthyl)-8-(2,6-dichlorophen-1-yl)-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene

Guidance literature:: Multi-step reaction with 2 steps

1: boron trifluoride diethyl etherate; triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

2: 18-crown-6 ether; potassium carbonate; thiophenol / N,N-dimethyl-formamide / 20 °C / Inert atmosphere

With 18-crown-6 ether; boron trifluoride diethyl etherate; potassium carbonate; thiophenol; triethylamine; In dichloromethane; N,N-dimethyl-formamide; 2: Michel-addition/Vicarious Nucleophilic Substitution styrylation;
DOI:10.1021/ol200148u