C₂₄H₂₈N₂O₆

Base Information

Chemical Name:C₂₄H₂₈N₂O₆
CAS No.:1332649-60-1
Molecular Formula:C₂₄H₂₈N₂O₆
Molecular Weight:440.496
Hs Code.:

C<sub>24</sub>H<sub>28</sub>N<sub>2</sub>O<sub>6</sub>

Synonyms:

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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 C₂₄H₂₈N₂O₆

Chemical Property:

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Technology Process of C₂₄H₂₈N₂O₆

There total 4 articles about C₂₄H₂₈N₂O₆ 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: 31.0%

: 93548-05-1
C₆H₈INO

: 875927-07-4
C₁₈H₂₁NO₅

: 1332649-60-1
C₂₄H₂₈N₂O₆

Guidance literature:: C₁₈H₂₁NO₅; With sodium hydride; In tetrahydrofuran; at 0 ℃;

C₆H₈INO; In tetrahydrofuran; at 40 ℃;
DOI:10.1111/j.1747-0285.2011.01133.x

Reference yield:

: 630-19-3
pivalaldehyde

: 1332649-60-1
C₂₄H₂₈N₂O₆

Guidance literature:: Multi-step reaction with 4 steps

1.1: Petroleum ether / Reflux

2.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 20 °C

3.1: potassium tert-butylate / tert-butyl alcohol / Reflux

4.1: sodium hydride / tetrahydrofuran / 0 °C

4.2: 40 °C

With dmap; potassium tert-butylate; sodium hydride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; Petroleum ether; tert-butyl alcohol; 3.1: Dieckmann reaction;
DOI:10.1111/j.1747-0285.2011.01133.x

Reference yield:

: 190080-34-3
(2RS,5S)-2-(tert-butyl)-5-methoxycarbonyl-1,3-oxazolidine

: 1332649-60-1
C₂₄H₂₈N₂O₆

Guidance literature:: Multi-step reaction with 3 steps

1.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 20 °C

2.1: potassium tert-butylate / tert-butyl alcohol / Reflux

3.1: sodium hydride / tetrahydrofuran / 0 °C

3.2: 40 °C

With dmap; potassium tert-butylate; sodium hydride; dicyclohexyl-carbodiimide; In tetrahydrofuran; dichloromethane; tert-butyl alcohol; 2.1: Dieckmann reaction;
DOI:10.1111/j.1747-0285.2011.01133.x