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methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate

Base Information Edit
  • Chemical Name:methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate
  • CAS No.:102437-56-9
  • Molecular Formula:C18H24O5S
  • Molecular Weight:352.452
  • Hs Code.:
  • Mol file:102437-56-9.mol
methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate

Synonyms:methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate

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Chemical Property of methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate Edit
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Technology Process of methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate

There total 4 articles about methyl 4-allyl-3-(tosyloxy)cyclohexanecarboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 5 steps
1: H2 / 5percent Rh/Al2O3 / methanol / 24 h / 25 °C / 2585.7 Torr
2: H2SO4 / 20 h / Heating
3: Celite, pyridinium chlorochromate (PCC) / CH2Cl2 / 3 h / 25 °C
4: 1.) 2,2-dimethoxypropane, p-toluenesulfonic acid, 2.) NaBH4 / 1.) benzene, reflux, 2.) methanol, 0 deg C, 30 min
5: 55 percent / pyridine / 144 h / 25 °C
With pyridine; sodium tetrahydroborate; Celite; sulfuric acid; hydrogen; toluene-4-sulfonic acid; 2,2-dimethoxy-propane; pyridinium chlorochromate; Rh/Al2O3; In methanol; dichloromethane;
DOI:10.1021/jo00362a012
Guidance literature:
Multi-step reaction with 3 steps
1: Celite, pyridinium chlorochromate (PCC) / CH2Cl2 / 3 h / 25 °C
2: 1.) 2,2-dimethoxypropane, p-toluenesulfonic acid, 2.) NaBH4 / 1.) benzene, reflux, 2.) methanol, 0 deg C, 30 min
3: 55 percent / pyridine / 144 h / 25 °C
With pyridine; sodium tetrahydroborate; Celite; toluene-4-sulfonic acid; 2,2-dimethoxy-propane; pyridinium chlorochromate; In dichloromethane;
DOI:10.1021/jo00362a012
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