2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

Base Information

Chemical Name:2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione
CAS No.:1401067-72-8
Molecular Formula:C₂₄H₃₀N₂O₅Si
Molecular Weight:454.598
Hs Code.:

Synonyms:2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

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Technology Process of 2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

There total 3 articles about 2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione 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: 62.0%

: 1401067-58-0
2-(4-hydroxy-4-(2-nitrophenyl)butyl)isoindoline-1,3-dione

: 18162-48-6
tert-butyldimethylsilyl chloride

: 1401067-72-8
2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 18h; Inert atmosphere;
DOI:10.1021/ja3072397

Reference yield:

: 32464-55-4
2-(4,4-diethoxybutyl)isoindoline-1,3-dione

: 1401067-72-8
2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogenchloride / water; acetone / 2 h / Inert atmosphere; Reflux

2.1: phenylmagnesium chloride / tetrahydrofuran / 0.5 h / -40 °C / Inert atmosphere

2.2: 0.5 h / -40 °C / Inert atmosphere

3.1: 1H-imidazole / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere

With 1H-imidazole; hydrogenchloride; phenylmagnesium chloride; In tetrahydrofuran; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja3072397

Reference yield:

: 22509-74-6
N-ethoxycarbonylphthalimide

: 1401067-72-8
2-(4-((tert-butyldimethylsilyl)oxy)-4-(2-nitrophenyl)butyl)-isoindoline-1,3-dione

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / tetrahydrofuran / 20 h / 20 °C / Inert atmosphere

2.1: hydrogenchloride / water; acetone / 2 h / Inert atmosphere; Reflux

3.1: phenylmagnesium chloride / tetrahydrofuran / 0.5 h / -40 °C / Inert atmosphere

3.2: 0.5 h / -40 °C / Inert atmosphere

4.1: 1H-imidazole / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere

With 1H-imidazole; hydrogenchloride; phenylmagnesium chloride; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/ja3072397