[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

Base Information

Chemical Name:[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine
CAS No.:213611-72-4
Molecular Formula:C₂₆H₄₀N₂O₆S
Molecular Weight:508.679
Hs Code.:

Synonyms:[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

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Chemical Property of [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

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Technology Process of [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

There total 3 articles about [2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine 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: 58.0%

: 213611-71-3
[2R,2(1S),4R]-4-ethyl-3-(2-nitrobenzenesulfonyl)-2-(1-nonyl-2-oxocyclopentyl)-1,3-oxazolidine

: 74-88-4
methyl iodide

: 213611-72-4
[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

Guidance literature:: With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; potassium tert-butylate; In tetrahydrofuran; at -78 - 20 ℃; for 18h;
DOI:10.1016/S0040-4020(98)00488-8

Reference yield:

: 213611-68-8
(2SR,4R)-4-ethyl-2-methoxy-3-(4-nitrobenzenesulfonyl)-1,3-oxazolidine

: 213611-72-4
[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 38 percent / BF₃*Et₂O / CH₂Cl₂ / 2 h / 20 °C

2: 58 percent / KO(t-Bu); DMPU / tetrahydrofuran / 18 h / -78 - 20 °C

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; boron trifluoride diethyl etherate; potassium tert-butylate; In tetrahydrofuran; dichloromethane; 1: Condensation / 2: Methylation;
DOI:10.1016/S0040-4020(98)00488-8

Reference yield:

: trimethyl-(2-nonyl-cyclopent-1-enyloxy)-silane

: 213611-72-4
[2R,2(1S,3R),4R]-4-ethyl-2-(3-methyl-1-nonyl-2-oxocyclopentyl)-3-(2-nitrobenzenesulfonyl)-1,3-oxazolidine

Guidance literature:: Multi-step reaction with 2 steps

1: 38 percent / BF₃*Et₂O / CH₂Cl₂ / 2 h / 20 °C

2: 58 percent / KO(t-Bu); DMPU / tetrahydrofuran / 18 h / -78 - 20 °C

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; boron trifluoride diethyl etherate; potassium tert-butylate; In tetrahydrofuran; dichloromethane; 1: Condensation / 2: Methylation;
DOI:10.1016/S0040-4020(98)00488-8