2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

Base Information

Chemical Name:2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one
CAS No.:1616480-49-9
Molecular Formula:C₂₀H₁₇F₃INO₃
Molecular Weight:503.26
Hs Code.:

Synonyms:2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

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Chemical Property of 2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

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Technology Process of 2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

There total 6 articles about 2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one 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:

: 1616480-48-8
2,2,2-trifluoro-1-(7-hydroxy-8-iodo-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl)ethan-1-one

: 70-11-1
α-bromoacetophenone

: 1616480-49-9
2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 16h;

Reference yield:

: 4424-20-8
2,3,4,5-tetrahydro-1H-3-benzazepine

: 1616480-49-9
2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid; trifluoroacetic acid / 1.25 h / 0 °C

1.2: 3 h / 0 - 20 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.5 h / 0 - 20 °C

3.1: palladium 10% on activated carbon; ammonium formate / tetrahydrofuran / 3 h / Inert atmosphere; Reflux

4.1: sulfuric acid; sodium nitrite / water / 1 h / 70 °C

5.1: N-iodo-succinimide; trifluoroacetic acid / chloroform / 0.5 h / 20 °C

6.1: potassium carbonate / acetone / 16 h / 20 °C

With N-iodo-succinimide; sulfuric acid; palladium 10% on activated carbon; ammonium formate; potassium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; sodium nitrite; In tetrahydrofuran; dichloromethane; chloroform; water; acetone;

Reference yield:

: 163068-05-1
3-(trifluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepine-7-amine

: 1616480-49-9
2,2,2-trifluoro-1-[7-iodo-8-(2-oxo-2-phenylethoxy)-1,2,4,5-tetrahydrobenzo[d]azepin-3-yl]ethan-1-one

Guidance literature:: Multi-step reaction with 3 steps

1: sulfuric acid; sodium nitrite / water / 1 h / 70 °C

2: N-iodo-succinimide; trifluoroacetic acid / chloroform / 0.5 h / 20 °C

3: potassium carbonate / acetone / 16 h / 20 °C

With N-iodo-succinimide; sulfuric acid; potassium carbonate; trifluoroacetic acid; sodium nitrite; In chloroform; water; acetone;