Technology Process of C18H28O4
There total 10 articles about C18H28O4 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
oxalyl dichloride; dimethyl sulfoxide; triethylamine;
In
dichloromethane;
at -78 ℃;
for 1h;
DOI:10.1016/j.tetlet.2011.03.089
- Guidance literature:
-
Multi-step reaction with 6 steps
1: 1,8-diazabicyclo[5.4.0]undec-7-ene; lithium chloride / dimethyl sulfoxide / 0.25 h / 0 °C
2: methanol; copper diacetate; ammonium chloride / dimethyl sulfoxide / 24 h / 20 °C
3: sodium tetrahydroborate; nickel (II) chloride hexahydrate / methanol / 3 h / 0 - 20 °C
4: N-ethyl-N,N-diisopropylamine / dichloromethane / 6 h / 0 - 20 °C
5: diisobutylaluminium hydride / dichloromethane / 0.25 h / 0 °C
6: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / 1 h / -78 °C
With
methanol; sodium tetrahydroborate; oxalyl dichloride; nickel (II) chloride hexahydrate; copper diacetate; diisobutylaluminium hydride; ammonium chloride; dimethyl sulfoxide; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; N-ethyl-N,N-diisopropylamine; lithium chloride;
In
methanol; dichloromethane; dimethyl sulfoxide;
1: Horner-Wadsworth-Emmons olefination / 6: Swern oxidation;
DOI:10.1016/j.tetlet.2011.03.089
- Guidance literature:
-
Multi-step reaction with 4 steps
1: sodium tetrahydroborate; nickel (II) chloride hexahydrate / methanol / 3 h / 0 - 20 °C
2: N-ethyl-N,N-diisopropylamine / dichloromethane / 6 h / 0 - 20 °C
3: diisobutylaluminium hydride / dichloromethane / 0.25 h / 0 °C
4: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / 1 h / -78 °C
With
sodium tetrahydroborate; oxalyl dichloride; nickel (II) chloride hexahydrate; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; N-ethyl-N,N-diisopropylamine;
In
methanol; dichloromethane;
4: Swern oxidation;
DOI:10.1016/j.tetlet.2011.03.089