Technology Process of 1,4-Benzenediol, 2-methyl-5-(1,2,2-trimethylcyclopentyl)-, (R)-
There total 19 articles about 1,4-Benzenediol, 2-methyl-5-(1,2,2-trimethylcyclopentyl)-, (R)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
(1S,2S)-2-(2,5-Dimethoxy-4-methyl-phenyl)-1,2-dimethyl-cyclopentanecarbaldehyde;
With
hydrazine dihydrochloride; hydrazine;
In
diethylene glycol;
at 125 ℃;
With
potassium hydroxide;
at 210 ℃;
With
boron tribromide;
In
dichloromethane;
at -70 - 20 ℃;
DOI:10.1016/S0040-4039(02)02674-6
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 80 percent / LDA / tetrahydrofuran / 8 h / -70 - 20 °C
2: 100 percent / PhCH=Ru(Cl)2(PCy3)2 / CH2Cl2 / 5 h / 20 °C
3: 85 percent / LDA / tetrahydrofuran; hexamethylphosphoric acid triamide / 12 h / -30 - 20 °C
4: H2 / 10 percent Pd-C / ethanol / 3 h
5: LAH / diethyl ether / 0.33 h / 0 °C
6: PCC; silica gel / CH2Cl2 / 1 h / 20 °C
7: N2H4*H2O; KOH / various solvent(s) / 12 h / 190 °C
8: 98 percent / BBr3 / CH2Cl2 / 2 h / -70 - 20 °C
With
potassium hydroxide; lithium aluminium tetrahydride; hydrogen; silica gel; boron tribromide; hydrazine hydrate; pyridinium chlorochromate; lithium diisopropyl amide;
palladium on activated charcoal; Grubbs catalyst first generation;
In
tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; ethanol; dichloromethane;
DOI:10.1016/j.tetlet.2005.06.156