Technology Process of trans-methyl 4-oxo-2-phenylchromane-3-carboxylate
There total 7 articles about trans-methyl 4-oxo-2-phenylchromane-3-carboxylate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: potassium carbonate; sodium iodide / acetone / 0.08 h / 20 °C / Inert atmosphere
1.2: 24 h / 65 °C
2.1: sodium hydride / 1,2-dimethoxyethane; mineral oil / 0.17 h / 0 - 20 °C / Inert atmosphere
2.2: 6 h / Reflux
3.1: p-nitrobenzenesulfonyl azide; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 3 h / 20 °C
4.1: Rh2[(N-(4-dodecylphenyl)sulfonyl)-(S)-prolinate]4 / toluene / 1.5 h / 0 °C / Inert atmosphere
5.1: chromium(VI) oxide; periodic acid / acetonitrile / 1 h / 20 °C
With
chromium(VI) oxide; p-nitrobenzenesulfonyl azide; Rh2[(N-(4-dodecylphenyl)sulfonyl)-(S)-prolinate]4; sodium hydride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; periodic acid; sodium iodide;
In
1,2-dimethoxyethane; dichloromethane; acetone; toluene; acetonitrile; mineral oil;
DOI:10.1016/j.tet.2011.03.004
- Guidance literature:
-
Multi-step reaction with 2 steps
1: Rh2[(N-(4-dodecylphenyl)sulfonyl)-(S)-prolinate]4 / toluene / 1.5 h / 0 °C / Inert atmosphere
2: chromium(VI) oxide; periodic acid / acetonitrile / 1 h / 20 °C
With
chromium(VI) oxide; Rh2[(N-(4-dodecylphenyl)sulfonyl)-(S)-prolinate]4; periodic acid;
In
toluene; acetonitrile;
DOI:10.1016/j.tet.2011.03.004