Technology Process of Toluene-4-sulfonic acid (E)-(3R,6R)-6-((1aR,3aR,3bS,5aR,6R,8aS,8bS,10R,10aR)-10-hydroxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2,3-dimethyl-hept-4-enyl ester
There total 5 articles about Toluene-4-sulfonic acid (E)-(3R,6R)-6-((1aR,3aR,3bS,5aR,6R,8aS,8bS,10R,10aR)-10-hydroxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2,3-dimethyl-hept-4-enyl ester which
guide to synthetic route it.
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synthetic route:
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88247-65-8
Toluene-4-sulfonic acid (E)-(3R,6R)-6-((1aR,3aR,3bS,5aR,6R,8aS,8bS,10R,10aR)-10-hydroxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2,3-dimethyl-hept-4-enyl ester
- Guidance literature:
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Multi-step reaction with 5 steps
1: 1.) EtMgBr / 1.) THF, -15 deg C, 30 min, room temperature, 60 min, 2.) benzene, 0 deg C, 30 min
2: 1.06 g / H2 / Lindlar catalyst / ethyl acetate / 1 h / Ambient temperature
3: 65 percent / xylene; propionic acid / 3 h / Heating
4: 72 percent / di-isobutylaluminium hydride / toluene / 2 h / -35 °C
5: 300 mg / pyridine / 16 h / 4 °C
With
diisobutylaluminum hydride; ethylmagnesium bromide; hydrogen;
Lindlar's catalyst;
In
pyridine; propionic acid; ethyl acetate; toluene; xylene;
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88247-65-8
Toluene-4-sulfonic acid (E)-(3R,6R)-6-((1aR,3aR,3bS,5aR,6R,8aS,8bS,10R,10aR)-10-hydroxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2,3-dimethyl-hept-4-enyl ester
- Guidance literature:
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Multi-step reaction with 4 steps
1: 1.06 g / H2 / Lindlar catalyst / ethyl acetate / 1 h / Ambient temperature
2: 65 percent / xylene; propionic acid / 3 h / Heating
3: 72 percent / di-isobutylaluminium hydride / toluene / 2 h / -35 °C
4: 300 mg / pyridine / 16 h / 4 °C
With
diisobutylaluminum hydride; hydrogen;
Lindlar's catalyst;
In
pyridine; propionic acid; ethyl acetate; toluene; xylene;
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-
88247-65-8
Toluene-4-sulfonic acid (E)-(3R,6R)-6-((1aR,3aR,3bS,5aR,6R,8aS,8bS,10R,10aR)-10-hydroxy-3a,5a-dimethyl-hexadecahydro-cyclopenta[a]cyclopropa[2,3]cyclopenta[1,2-f]naphthalen-6-yl)-2,3-dimethyl-hept-4-enyl ester
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 65 percent / xylene; propionic acid / 3 h / Heating
2: 72 percent / di-isobutylaluminium hydride / toluene / 2 h / -35 °C
3: 300 mg / pyridine / 16 h / 4 °C
With
diisobutylaluminum hydride;
In
pyridine; propionic acid; toluene; xylene;