C₂₁H₂₅NO₆

Base Information

Chemical Name:C₂₁H₂₅NO₆
CAS No.:1355242-71-5
Molecular Formula:C₂₁H₂₅NO₆
Molecular Weight:387.433
Hs Code.:

C<sub>21</sub>H<sub>25</sub>NO<sub>6</sub>

Synonyms:C₂₁H₂₅NO₆

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Chemical Property of C₂₁H₂₅NO₆

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Technology Process of C₂₁H₂₅NO₆

There total 2 articles about C₂₁H₂₅NO₆ 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: 66.0%

: 1355242-72-6
C₂₀H₂₅NO₇

: 90965-06-3
dimethyl 1-(1-diazo-2-oxopropyl)phosphonate

: 1355242-71-5
C₂₁H₂₅NO₆

Guidance literature:: C₂₀H₂₅NO₇; With potassium carbonate; In methanol; at 20 ℃; for 0.166667h;

dimethyl 1-(1-diazo-2-oxopropyl)phosphonate; In methanol; at 20 ℃; for 2h;
DOI:10.1021/ja2104679

Reference yield:

: 1355242-69-1
C₂₀H₂₇NO₇

: 1355242-71-5
C₂₁H₂₅NO₆

Guidance literature:: Multi-step reaction with 2 steps

2.1: potassium carbonate / methanol / 0.17 h / 20 °C

2.2: 2 h / 20 °C

With potassium carbonate; In methanol; 1.1: Swern oxidation;
DOI:10.1021/ja2104679

Reference yield:

: 1355242-71-5
C₂₁H₂₅NO₆

: 1355242-78-2
C₃₆H₄₁F₆N₅O₁₀

Guidance literature:: Multi-step reaction with 6 steps

1: copper(II) sulfate; sodium L-ascorbate / methanol; water

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 20 h / 0 - 4 °C

3: lithium perchlorate / acetonitrile / 20 h / 70 °C

4: triethylamine / dichloromethane / 20 h

5: palladium 10% on activated carbon; hydrogen / methanol / 5 h

6: triethylamine / dichloromethane / 20 h

With palladium 10% on activated carbon; hydrogen; lithium perchlorate; copper(II) sulfate; sodium L-ascorbate; triethylamine; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane; water; acetonitrile;
DOI:10.1021/ja2104679