Technology Process of 2β-(p-methylbenzyl)-3,4β-oxidopyrrolidine
There total 5 articles about 2β-(p-methylbenzyl)-3,4β-oxidopyrrolidine which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogen;
palladium on activated charcoal;
In
ethanol;
for 1.5h;
DOI:10.1021/ja00386a039
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 71 percent / zinc dust, aq. HCl / ethanol / 1.) 1.5 h, 2.) reflux, 1.5 h
2: 93 percent / aq. NaOH / toluene / 1 h / 3 - 5 °C
3: 78 percent / N-iodosuccinimide, aq. perchloric acid / tetrahydrofuran / 1.) 3-5 deg C, 1 h, 2.) 3-5 deg C -> room temperature, 1 h
4: 90 percent / 5percent KOH, MeOH / 0.5 h
5: 95 percent / hydrogen / 10percent Pd/C / ethanol / 1.5 h
With
hydrogenchloride; methanol; potassium hydroxide; sodium hydroxide; N-iodo-succinimide; perchloric acid; hydrogen; zinc;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol; toluene;
DOI:10.1021/ja00386a039
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 93 percent / aq. NaOH / toluene / 1 h / 3 - 5 °C
2: 78 percent / N-iodosuccinimide, aq. perchloric acid / tetrahydrofuran / 1.) 3-5 deg C, 1 h, 2.) 3-5 deg C -> room temperature, 1 h
3: 90 percent / 5percent KOH, MeOH / 0.5 h
4: 95 percent / hydrogen / 10percent Pd/C / ethanol / 1.5 h
With
methanol; potassium hydroxide; sodium hydroxide; N-iodo-succinimide; perchloric acid; hydrogen;
palladium on activated charcoal;
In
tetrahydrofuran; ethanol; toluene;
DOI:10.1021/ja00386a039