Technology Process of 3-Cyclohexene-1-ethanol, 2,2,3-trimethyl-, acetate, (R)-
There total 8 articles about 3-Cyclohexene-1-ethanol, 2,2,3-trimethyl-, acetate, (R)- which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1: 78 percent / 40 percent peracetic acid/AcOH, Na2CO3, EDTA tetrasodium salt / toluene / Ambient temperature
2: 75 percent / ZnBr2 / toluene / Heating
3: 97 percent / LiAlH4 / diethyl ether / 1.) reflux, 2.) r.t., 1 h
4: 87 percent / conc. H3PO4 / 2 h / 60 °C
6: 95 percent / hydrogen / Raney-Ni / ethanol / 8 h / Ambient temperature
7: 72 percent / t-BuOK / toluene / 3 h / Heating
8: 70 percent / TsOH / toluene / 2 h / Heating
With
peracetic acid; lithium aluminium tetrahydride; phosphoric acid; potassium tert-butylate; hydrogen; ethylene diamine tetraacetic acid tetrasodium salt; sodium carbonate; toluene-4-sulfonic acid; acetic acid; zinc dibromide;
nickel;
In
diethyl ether; ethanol; toluene;
DOI:10.1002/hlca.19920750507
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 87 percent / conc. H3PO4 / 2 h / 60 °C
3: 95 percent / hydrogen / Raney-Ni / ethanol / 8 h / Ambient temperature
4: 72 percent / t-BuOK / toluene / 3 h / Heating
5: 70 percent / TsOH / toluene / 2 h / Heating
With
phosphoric acid; potassium tert-butylate; hydrogen; toluene-4-sulfonic acid;
nickel;
In
ethanol; toluene;
DOI:10.1002/hlca.19920750507