Technology Process of 3-acetyl-isoaltholactone
There total 10 articles about 3-acetyl-isoaltholactone which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 10 steps
1: 74 percent / pyridinium toluene-p-sulphonate / CH2Cl2 / 3 h / 25 °C
2: 78 percent / NaBH4; CeCl3*7H2O / methanol / -40 - 20 °C
3: 2.8 g / Ph3P; DEAD / tetrahydrofuran / 0 - 20 °C
4: 82 percent / K2CO3 / methanol / 10 h / 20 °C
5: 95 percent / Et3N; DMAP / CH2Cl2 / 8 h / 0 °C
6: 82 percent / NaHCO3; p-CPBA / CH2Cl2 / 10 h / 25 °C
7: 80 percent / TBAF / tetrahydrofuran / 2 h / 25 °C
8: 90 percent / PPTS / CH2Cl2 / 4 h / 25 °C
9: 92 percent / 4-dimethylaminopyridine; pyridine / CH2Cl2 / 5 h / 25 °C
10: 83 percent / CrO3; HOAc / 5 h / 25 °C
With
pyridine; chromium(VI) oxide; dmap; sodium tetrahydroborate; cerium(III) chloride; p-chloroperbenzoic acid; tetrabutyl ammonium fluoride; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; diethylazodicarboxylate;
In
tetrahydrofuran; methanol; dichloromethane;
3: Mitsunobu reaction;
DOI:10.1016/S0040-4020(02)00791-3
- Guidance literature:
-
Multi-step reaction with 9 steps
1: 78 percent / NaBH4; CeCl3*7H2O / methanol / -40 - 20 °C
2: 2.8 g / Ph3P; DEAD / tetrahydrofuran / 0 - 20 °C
3: 82 percent / K2CO3 / methanol / 10 h / 20 °C
4: 95 percent / Et3N; DMAP / CH2Cl2 / 8 h / 0 °C
5: 82 percent / NaHCO3; p-CPBA / CH2Cl2 / 10 h / 25 °C
6: 80 percent / TBAF / tetrahydrofuran / 2 h / 25 °C
7: 90 percent / PPTS / CH2Cl2 / 4 h / 25 °C
8: 92 percent / 4-dimethylaminopyridine; pyridine / CH2Cl2 / 5 h / 25 °C
9: 83 percent / CrO3; HOAc / 5 h / 25 °C
With
pyridine; chromium(VI) oxide; dmap; sodium tetrahydroborate; cerium(III) chloride; p-chloroperbenzoic acid; tetrabutyl ammonium fluoride; pyridinium p-toluenesulfonate; sodium hydrogencarbonate; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; diethylazodicarboxylate;
In
tetrahydrofuran; methanol; dichloromethane;
2: Mitsunobu reaction;
DOI:10.1016/S0040-4020(02)00791-3