Technology Process of 3a-cyclopropyl-2-methoxycarbonyl-4-oxo-2-phenyl-4H-2,3,3a,11c-tetrahydropyrro<1,3-d>naphtho<2,1-b>pyran
There total 17 articles about 3a-cyclopropyl-2-methoxycarbonyl-4-oxo-2-phenyl-4H-2,3,3a,11c-tetrahydropyrro<1,3-d>naphtho<2,1-b>pyran which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1.) n-butyl lithium / 1.) 4 h, r.t., ether, hexan; 2.) ether, r.t., 15 h
2: 69 percent / sodium hydroxide / H2O; ethanol / 3 h / Heating
3: 1.) dicyclohexylcarbodiimide, p-toluenesulphonic acid; 2.) g. acetic acid / 1.) pyridine, 24 h; 2.) 2 h, r.t., 0 degC, overnight
4: 95 percent / sodium sulphate / CH2Cl2 / reflux 1 h, r.t. 10 h
5: xylene / 24 h / Heating
With
sodium hydroxide; n-butyllithium; toluene-4-sulfonic acid; acetic acid; sodium sulfate; dicyclohexyl-carbodiimide;
In
ethanol; dichloromethane; water; xylene;
DOI:10.1016/S0040-4020(01)85931-7
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 1.) dicyclohexylcarbodiimide, p-toluenesulphonic acid; 2.) g. acetic acid / 1.) pyridine, 24 h; 2.) 2 h, r.t., 0 degC, overnight
2: 95 percent / sodium sulphate / CH2Cl2 / reflux 1 h, r.t. 10 h
3: xylene / 24 h / Heating
With
toluene-4-sulfonic acid; acetic acid; sodium sulfate; dicyclohexyl-carbodiimide;
In
dichloromethane; xylene;
DOI:10.1016/S0040-4020(01)85931-7
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 69 percent / sodium hydroxide / H2O; ethanol / 3 h / Heating
2: 1.) dicyclohexylcarbodiimide, p-toluenesulphonic acid; 2.) g. acetic acid / 1.) pyridine, 24 h; 2.) 2 h, r.t., 0 degC, overnight
3: 95 percent / sodium sulphate / CH2Cl2 / reflux 1 h, r.t. 10 h
4: xylene / 24 h / Heating
With
sodium hydroxide; toluene-4-sulfonic acid; acetic acid; sodium sulfate; dicyclohexyl-carbodiimide;
In
ethanol; dichloromethane; water; xylene;
DOI:10.1016/S0040-4020(01)85931-7