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((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid

Base Information
  • Chemical Name:((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid
  • CAS No.:374782-82-8
  • Molecular Formula:C12H20O2
  • Molecular Weight:196.29
  • Hs Code.:
((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid

Synonyms:((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid

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Chemical Property of ((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid
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Technology Process of ((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid

There total 11 articles about ((R)-1,3,3-Trimethyl-2-methylene-cyclohexyl)-acetic acid 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 10 steps
1: diethyl ether / 0 - 20 °C
2: 750 mg / PCC; silica gel / CH2Cl2 / 12 h
3: 90 percent / NBS / CH2Cl2; methanol / 6 h / 0 - 5 °C
4: 76 percent / potassium tert-butoxide / tetrahydrofuran / -5 - 20 °C
5: O3; NaHCO3 / CH2Cl2 / 0.08 h / -70 °C
6: 93 mg / Ac2O; Et3N; 4-N,N-(dimethylamino)pyridine / benzene / 6 h / Heating
7: 90 percent / H2 / Pd/C / ethyl acetate / 0.5 h
8: 60 percent Turnov. / BF3*OEt2 / benzene / 2 h / 0 - 5 °C
9: 90 percent / Raney Ni / ethanol / 0.5 h / Heating
10: 94 percent / aq. NaOH / methanol / 12 h / Heating
With dmap; sodium hydroxide; N-Bromosuccinimide; boron trifluoride diethyl etherate; potassium tert-butylate; hydrogen; acetic anhydride; silica gel; nickel; sodium hydrogencarbonate; ozone; triethylamine; pyridinium chlorochromate; palladium on activated charcoal; In tetrahydrofuran; methanol; diethyl ether; ethanol; dichloromethane; ethyl acetate; benzene; 6: Criegee rearrangement;
DOI:10.1021/jo0105484
Guidance literature:
Multi-step reaction with 4 steps
1: 90 percent / H2 / Pd/C / ethyl acetate / 0.5 h
2: 60 percent Turnov. / BF3*OEt2 / benzene / 2 h / 0 - 5 °C
3: 90 percent / Raney Ni / ethanol / 0.5 h / Heating
4: 94 percent / aq. NaOH / methanol / 12 h / Heating
With sodium hydroxide; boron trifluoride diethyl etherate; hydrogen; nickel; palladium on activated charcoal; In methanol; ethanol; ethyl acetate; benzene;
DOI:10.1021/jo0105484
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