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Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester

Base Information Edit
  • Chemical Name:Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester
  • CAS No.:93489-68-0
  • Molecular Formula:C21H30O3
  • Molecular Weight:330.467
  • Hs Code.:
  • Mol file:93489-68-0.mol
Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester

Synonyms:

Suppliers and Price of Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester
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Chemical Property of Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester Edit
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Technology Process of Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester

There total 10 articles about Benzoic acid (R)-3-((1R,3aR,4S,7aR)-4-hydroxy-7a-methyl-octahydro-inden-1-yl)-butyl ester 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 4 steps
1: t-BuOK / tetrahydrofuran / 63 h / Ambient temperature
2: 70 percent / 0.813M BF3*Et2O / CH2Cl2 / 2 h
3: 77 percent / H2 / 5 percent Pd/C / ethyl acetate / 735.5 Torr
4: 1.) pyridine / 1.) 0 deg C, 1 h; 2.) water, 30 min
With pyridine; boron trifluoride diethyl etherate; potassium tert-butylate; hydrogen; palladium on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1016/0040-4020(84)80011-3
Guidance literature:
Multi-step reaction with 10 steps
2: 82 percent / H2 / 10percent Rh/C / ethyl acetate / 735.5 Torr
3: 57 percent / trifluoroperacetic acid, disodium hydrogen phosphate / CH2Cl2 / 1.) 0 deg C, 1 h; 2.) RT, 30 h
4: 80 percent / iodotrimethylsilane / CCl4 / 5 h / Ambient temperature
5: 97 percent / pyridinium chlorochromate; / CH2Cl2 / 2.5 h / Ambient temperature
6: 87 percent / 25percent NaOMe / methanol / 3.5 h
7: t-BuOK / tetrahydrofuran / 63 h / Ambient temperature
8: 70 percent / 0.813M BF3*Et2O / CH2Cl2 / 2 h
9: 77 percent / H2 / 5 percent Pd/C / ethyl acetate / 735.5 Torr
10: 1.) pyridine / 1.) 0 deg C, 1 h; 2.) water, 30 min
With pyridine; disodium hydrogenphosphate; trimethylsilyl iodide; trifluoroacetyl peroxide; boron trifluoride diethyl etherate; potassium tert-butylate; hydrogen; sodium methylate; pyridinium chlorochromate; palladium on activated charcoal; Rh on carbon; In tetrahydrofuran; methanol; tetrachloromethane; dichloromethane; ethyl acetate;
DOI:10.1016/0040-4020(84)80011-3
Guidance literature:
Multi-step reaction with 6 steps
1: 97 percent / pyridinium chlorochromate; / CH2Cl2 / 2.5 h / Ambient temperature
2: 87 percent / 25percent NaOMe / methanol / 3.5 h
3: t-BuOK / tetrahydrofuran / 63 h / Ambient temperature
4: 70 percent / 0.813M BF3*Et2O / CH2Cl2 / 2 h
5: 77 percent / H2 / 5 percent Pd/C / ethyl acetate / 735.5 Torr
6: 1.) pyridine / 1.) 0 deg C, 1 h; 2.) water, 30 min
With pyridine; boron trifluoride diethyl etherate; potassium tert-butylate; hydrogen; sodium methylate; pyridinium chlorochromate; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate;
DOI:10.1016/0040-4020(84)80011-3
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