C₂₀H₂₄O₆

Base Information

Chemical Name:C₂₀H₂₄O₆
CAS No.:1258238-35-5
Molecular Formula:C₂₀H₂₄O₆
Molecular Weight:360.407
Hs Code.:

C<sub>20</sub>H<sub>24</sub>O<sub>6</sub>

Synonyms:C₂₀H₂₄O₆

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Chemical Property of C₂₀H₂₄O₆

Chemical Property:

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Technology Process of C₂₀H₂₄O₆

There total 3 articles about C₂₀H₂₄O₆ 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: 82.0%

: 541-41-3
chloroformic acid ethyl ester

: 288632-71-3
(2-propynyl)-(phenylmethyl)-2,2-propanedioic acid diethyl ester

: 1258238-35-5
C₂₀H₂₄O₆

Guidance literature:: (2-propynyl)-(phenylmethyl)-2,2-propanedioic acid diethyl ester; With n-butyllithium; In tetrahydrofuran; at -78 ℃; for 1h; Inert atmosphere;

chloroformic acid ethyl ester; In tetrahydrofuran; at -78 - 20 ℃; Inert atmosphere;
DOI:10.1021/jo101709n

Reference yield:

: 17920-23-9
diethyl propargylmalonate

: 1258238-35-5
C₂₀H₂₄O₆

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / tetrahydrofuran / -20 - 20 °C / Inert atmosphere

1.2: 0 - 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

2.2: -78 - 20 °C / Inert atmosphere

With n-butyllithium; sodium hydride; In tetrahydrofuran;
DOI:10.1021/jo101709n

Reference yield:

: 100-39-0
benzyl bromide

: 1258238-35-5
C₂₀H₂₄O₆

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / tetrahydrofuran / -20 - 20 °C / Inert atmosphere

1.2: 0 - 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran / 1 h / -78 °C / Inert atmosphere

2.2: -78 - 20 °C / Inert atmosphere

With n-butyllithium; sodium hydride; In tetrahydrofuran;
DOI:10.1021/jo101709n