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2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl ester

Base Information
  • Chemical Name:2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl ester
  • CAS No.:135716-22-2
  • Molecular Formula:C28H50O6
  • Molecular Weight:482.701
  • Hs Code.:
2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl ester

Synonyms:2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl ester

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Chemical Property of 2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl ester
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Technology Process of 2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl ester

There total 21 articles about 2,2-Dimethyl-butyric acid (1S,2S,3S,6R)-2-[2-((4R,6R)-6-methoxycarbonylmethyl-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl]-3-methyl-6-propyl-cyclohexylmethyl 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 14 steps
1: BF3*Et2O
2: MeONa
3: ImH / dimethylformamide
4: lithium 4,4'-di-tert-butylbiphenyl / tetrahydrofuran / -78 °C
5: 1.) NaH, CS2, 2.) MeI, 3.) Bu3SnH / 2.) THF
6: aq. HF / acetonitrile
7: 48 h / 40 °C
9: LiI / hexamethylphosphoric acid triamide; toluene / Heating
10: Zn / methanol / Heating
11: K2CO3 / methanol / Ambient temperature
12: CSA / acetone
13: O3, Ph3P / CH2Cl2
14: 1.) KMnO4, NaH2PO4 / 1.) t-BuOH, H2O
With 1H-imidazole; carbon disulfide; potassium permanganate; sodium dihydrogenphosphate; boron trifluoride diethyl etherate; hydrogen fluoride; tri-n-butyl-tin hydride; sodium methylate; sodium hydride; lithium 4,4′-di-tert-butylbiphenylide; potassium carbonate; ozone; triphenylphosphine; lithium iodide; zinc; methyl iodide; camphor-10-sulfonic acid; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; acetonitrile;
DOI:10.1016/S0040-4039(00)75798-4
Guidance literature:
Multi-step reaction with 13 steps
1: MeONa
2: ImH / dimethylformamide
3: lithium 4,4'-di-tert-butylbiphenyl / tetrahydrofuran / -78 °C
4: 1.) NaH, CS2, 2.) MeI, 3.) Bu3SnH / 2.) THF
5: aq. HF / acetonitrile
6: 48 h / 40 °C
8: LiI / hexamethylphosphoric acid triamide; toluene / Heating
9: Zn / methanol / Heating
10: K2CO3 / methanol / Ambient temperature
11: CSA / acetone
12: O3, Ph3P / CH2Cl2
13: 1.) KMnO4, NaH2PO4 / 1.) t-BuOH, H2O
With 1H-imidazole; carbon disulfide; potassium permanganate; sodium dihydrogenphosphate; hydrogen fluoride; tri-n-butyl-tin hydride; sodium methylate; sodium hydride; lithium 4,4′-di-tert-butylbiphenylide; potassium carbonate; ozone; triphenylphosphine; lithium iodide; zinc; methyl iodide; camphor-10-sulfonic acid; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane; N,N-dimethyl-formamide; acetone; toluene; acetonitrile;
DOI:10.1016/S0040-4039(00)75798-4
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