2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane

Base Information

Chemical Name:2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane
CAS No.:1087041-21-1
Molecular Formula:C₁₅H₁₈FNO₄
Molecular Weight:295.311
Hs Code.:

Synonyms:2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane

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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-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane

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Technology Process of 2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane

There total 1 articles about 2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane 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: 60.0%

: 1087041-05-1
(R)-2-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-pent-4-enal

: 107-21-1
ethylene glycol

: 1087041-21-1
2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane

Guidance literature:: With toluene-4-sulfonic acid; orthoformic acid triethyl ester; In benzene; at 20 ℃;
DOI:10.1021/ol8023133

Reference yield: 80.0%

: 1087041-21-1
2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane

: 1087041-41-5
(3aR,5R,6S)-5-(1,3-dioxolan-2-yl)-6-(4-fluorophenyl)-3a,4,5,6-tetrahydro-3H-cyclopent[c]isoxazole

Guidance literature:: 2-((R)-1-[(S)-1-(4-fluorophenyl)-2-nitroethyl]-but-3-enyl)-1,3-dioxolane; With chloro-trimethyl-silane; triethylamine; In tetrahydrofuran; at -90 - 0 ℃; for 2h; Inert atmosphere;

With N,N,N,N,N,N-hexamethylphosphoric triamide; In tetrahydrofuran; at 20 ℃; for 15h; Inert atmosphere;

With hydrogenchloride; In tetrahydrofuran; water; at 0 ℃; for 1h; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/ol8023133