3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

Base Information

Chemical Name:3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole
CAS No.:1269103-88-9
Molecular Formula:C₂₇H₂₂N₂O₆S
Molecular Weight:502.547
Hs Code.:

Synonyms:3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

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Chemical Property of 3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

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Technology Process of 3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

There total 5 articles about 3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole 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: 93.0%

: 1269103-86-7
3-(1-hydroxyprop-2-yn-1-yl)-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

: 107-30-2
chloromethyl methyl ether

: 1269103-88-9
3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 50 ℃; for 12h; Inert atmosphere;
DOI:10.3987/COM-10-S(E)11

Reference yield:

: 1269103-82-3
2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

: 1269103-88-9
3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

Guidance literature:: Multi-step reaction with 3 steps

1: aluminum (III) chloride / dichloromethane / 1 h / -78 °C / Inert atmosphere

2: tetrahydrofuran / 2 h / 0 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 50 °C / Inert atmosphere

With aluminum (III) chloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; 2: Grignard reaction;
DOI:10.3987/COM-10-S(E)11

Reference yield:

: 23308-83-0
(2-nitrobenzyl)triphenylphosphonium bromide

: 1269103-88-9
3-[1-(methoxymethyloxy)prop-2-yn-1-yl]-2-[2-(2-nitrophenyl)ethenyl]-N-(phenylsulfonyl)indole

Guidance literature:: Multi-step reaction with 4 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0 - 20 °C / Inert atmosphere

1.2: 3 h / 20 °C / Inert atmosphere

2.1: aluminum (III) chloride / dichloromethane / 1 h / -78 °C / Inert atmosphere

3.1: tetrahydrofuran / 2 h / 0 °C / Inert atmosphere

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 12 h / 50 °C / Inert atmosphere

With aluminum (III) chloride; n-butyllithium; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; hexane; dichloromethane; 1.1: Wittig reaction / 1.2: Wittig reaction / 3.1: Grignard reaction;
DOI:10.3987/COM-10-S(E)11