Technology Process of 5-[(-)-(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy-methoxy]-2-(4-methoxyphenyl)-8,8-dimethyl-2,3-dihydro-8H-pyrano[2,3-f]chromen-4-one
There total 8 articles about 5-[(-)-(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy-methoxy]-2-(4-methoxyphenyl)-8,8-dimethyl-2,3-dihydro-8H-pyrano[2,3-f]chromen-4-one which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
5-hydroxy-2-(4-methoxyphenyl)-8,8-dimethyl-2,3-dihydro-8H-pyrano[2,3-f]chromen-4-one;
With
sodium hydroxide;
In
dichloromethane; water;
at 0 - 20 ℃;
for 0.5h;
(1R,2S,5R)-1-(chloromethoxy)-2-isopropyl-5-methylcyclohexane;
In
dichloromethane; water;
at 0 ℃;
for 0.5h;
Further stages.;
DOI:10.1002/jccs.200700119
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 94 percent / KOH / ethanol; H2O / 8 h / 20 °C
2.1: 90 percent / NaOH; Adogen 464 / benzylcinchonium salt / H2O; CH2Cl2 / 2 h / 60 °C
3.1: 96 percent / BBr3 / CH2Cl2 / 5 h / -23 °C
4.1: NaOH; Androgen 464 / CH2Cl2; H2O / 0.5 h / 0 - 20 °C
4.2: 100 percent / CH2Cl2; H2O / 0.5 h / 0 °C
With
potassium hydroxide; sodium hydroxide; adogen 464; boron tribromide;
benzylcinchonium salt;
In
ethanol; dichloromethane; water;
DOI:10.1002/jccs.200700119
- Guidance literature:
-
Multi-step reaction with 5 steps
1.2: 84 percent / DDQ
2.1: 94 percent / KOH / ethanol; H2O / 8 h / 20 °C
3.1: 90 percent / NaOH; Adogen 464 / benzylcinchonium salt / H2O; CH2Cl2 / 2 h / 60 °C
4.1: 96 percent / BBr3 / CH2Cl2 / 5 h / -23 °C
5.1: NaOH; Androgen 464 / CH2Cl2; H2O / 0.5 h / 0 - 20 °C
5.2: 100 percent / CH2Cl2; H2O / 0.5 h / 0 °C
With
potassium hydroxide; sodium hydroxide; adogen 464; boron tribromide;
benzylcinchonium salt;
In
ethanol; dichloromethane; water;
DOI:10.1002/jccs.200700119