C₂₀H₂₀N₂O₆

Base Information

Chemical Name:C₂₀H₂₀N₂O₆
CAS No.:130740-54-4
Molecular Formula:C₂₀H₂₀N₂O₆
Molecular Weight:384.389
Hs Code.:

C<sub>20</sub>H<sub>20</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 C₂₀H₂₀N₂O₆

Chemical Property:

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Technology Process of C₂₀H₂₀N₂O₆

There total 20 articles about C₂₀H₂₀N₂O₆ 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:

: 41717-28-6
2-benzofuroyl chloride

: 130740-54-4,130740-55-5,145629-13-6,145629-14-7
C₂₀H₂₀N₂O₆

Guidance literature:: Multi-step reaction with 6 steps

1: NaHCO₃ / CH₂Cl₂; H₂O / 1 h / Ambient temperature

2: LiOH / ethanol / 24 h / Ambient temperature

3: Et₃N / tetrahydrofuran / 1.5 h / 0 °C

4: tetrahydrofuran / 2 h / 0 °C

5: 50 percent / N-bromosuccinimide (NBS) / CHCl₃ / Ambient temperature

6: silver triflate / tetrahydrofuran; H₂O / 0.5 h / Ambient temperature

With lithium hydroxide; N-Bromosuccinimide; silver trifluoromethanesulfonate; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; chloroform; water;
DOI:10.1021/ja00055a025

Reference yield:

: 41717-28-6
2-benzofuroyl chloride

: 130740-54-4,130740-55-5,145629-13-6,145629-14-7
C₂₀H₂₀N₂O₆

Guidance literature:: Multi-step reaction with 6 steps

1: NaHCO₃ / CH₂Cl₂; H₂O / 1 h / Ambient temperature

2: LiOH / ethanol / 24 h / Ambient temperature

3: Et₃N / tetrahydrofuran / 1.5 h / 0 °C

4: tetrahydrofuran / 2 h / 0 °C

5: 50 percent / N-bromosuccinimide (NBS) / CHCl₃ / Ambient temperature

6: silver triflate / tetrahydrofuran; H₂O / 0.5 h / Ambient temperature

With lithium hydroxide; N-Bromosuccinimide; silver trifluoromethanesulfonate; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; ethanol; dichloromethane; chloroform; water;
DOI:10.1021/ja00055a025

Reference yield:

: 130740-51-1
N--N-(4-methoxybenzyl)glycine

: 130740-54-4,130740-55-5,145629-13-6,145629-14-7
C₂₀H₂₀N₂O₆

Guidance literature:: Multi-step reaction with 4 steps

1: Et₃N / tetrahydrofuran / 1.5 h / 0 °C

2: tetrahydrofuran / 2 h / 0 °C

3: 50 percent / N-bromosuccinimide (NBS) / CHCl₃ / Ambient temperature

4: silver triflate / tetrahydrofuran; H₂O / 0.5 h / Ambient temperature

With N-Bromosuccinimide; silver trifluoromethanesulfonate; triethylamine; In tetrahydrofuran; chloroform; water;
DOI:10.1021/ja00055a025