2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

Base Information

Chemical Name:2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one
CAS No.:1542158-88-2
Molecular Formula:C₂₅H₁₉I₂NO₄
Molecular Weight:651.239
Hs Code.:

Synonyms:2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

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Chemical Property of 2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

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Technology Process of 2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

There total 3 articles about 2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)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: 87.0%

: 75-52-5
nitromethane

: 1542159-03-4
C₂₄H₁₆I₂O₂

: 1542158-88-2
2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

Guidance literature:: With N-(9-epi-hydroquinidin-9-yl)-N'-[3,5-bis(CF₃)phenyl]thiourea; In toluene; at 40 ℃; for 36h; enantioselective reaction; Molecular sieve;
DOI:10.1002/ejoc.201301860

Reference yield:

: 67717-18-4
1-(4-iodophenyl)-2-(triphenylphosphoranylidene)ethan-1-one

: 1542158-88-2
2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 16 h / Reflux

2: N-(9-epi-hydroquinidin-9-yl)-N'-[3,5-bis(CF₃)phenyl]thiourea / toluene / 36 h / 40 °C / Molecular sieve

With N-(9-epi-hydroquinidin-9-yl)-N'-[3,5-bis(CF₃)phenyl]thiourea; In dichloromethane; toluene; 2: |Michael Addition;
DOI:10.1002/ejoc.201301860

Reference yield:

: 643-79-8
o-phthalic dicarboxaldehyde

: 1542158-88-2
2-((1R,2R,3S)-2-(4-iodobenzoyl)-3-(nitromethyl)-2,3-dihydro-1H-inden-1-yl)-1-(4-iodophenyl)ethan-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: dichloromethane / 16 h / Reflux

2: N-(9-epi-hydroquinidin-9-yl)-N'-[3,5-bis(CF₃)phenyl]thiourea / toluene / 36 h / 40 °C / Molecular sieve

With N-(9-epi-hydroquinidin-9-yl)-N'-[3,5-bis(CF₃)phenyl]thiourea; In dichloromethane; toluene; 2: |Michael Addition;
DOI:10.1002/ejoc.201301860