N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

Base Information

Chemical Name:N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine
CAS No.:910378-86-8
Molecular Formula:C₂₄H₃₂N₂O₅
Molecular Weight:428.528
Hs Code.:

Synonyms:N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

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Chemical Property of N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

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Technology Process of N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

There total 3 articles about N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine 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: 42.0%

: 910378-84-6
2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

: 13288-06-7
1-(2-bromoethoxy)-4-nitrobenzene

: 910378-86-8
N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

Guidance literature:: With tetra-(n-butyl)ammonium iodide; potassium carbonate; In acetonitrile; at 50 ℃; for 24h;
DOI:10.1016/j.bmc.2006.05.065

Reference yield:

: 910378-83-5
3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-5-(2-nitroethyl)-2H-1-benzopyran

: 910378-86-8
N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / LiAlH₄ / tetrahydrofuran / 2 h / Heating

2: 42 percent / K₂CO₃; tetra-n-butylammonium iodide / acetonitrile / 24 h / 50 °C

With lithium aluminium tetrahydride; tetra-(n-butyl)ammonium iodide; potassium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1016/j.bmc.2006.05.065

Reference yield:

: 389633-98-1
3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-benzopyran-5-carboxaldehyde

: 910378-86-8
N-[2-(4-nitrophenoxy)ethyl]-2-(3,4-dihydro-6-methoxy-2,2,7,8-tetramethyl-2H-1-benzopyran-5-yl)ethylamine

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / ammonium acetate / 2 h / 100 °C

2: 98 percent / LiAlH₄ / tetrahydrofuran / 2 h / Heating

3: 42 percent / K₂CO₃; tetra-n-butylammonium iodide / acetonitrile / 24 h / 50 °C

With ammonium acetate; lithium aluminium tetrahydride; tetra-(n-butyl)ammonium iodide; potassium carbonate; In tetrahydrofuran; acetonitrile;
DOI:10.1016/j.bmc.2006.05.065