(R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

Base Information

Chemical Name:(R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol
CAS No.:122854-68-6
Molecular Formula:C₁₅H₂₆O₄
Molecular Weight:270.369
Hs Code.:

Synonyms:(R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

Suppliers and Price of (R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

There total 1 articles about (R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol 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:

Reference yield: 88.0%

: 2457-93-4
(3aR,5S,6aR)-2,2-dimethyl-5-[(2R)-oxiran-2-yl]-3a,5,6,6a-tetrahydrofuro[2,3-d] [1,3]dioxole

: 931-50-0
cyclohexylmagnesium bromide

: 122854-68-6
(R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

Guidance literature:: With copper(l) iodide; In tetrahydrofuran; -20 to -15 deg C, 1 h, -10 to 0 deg C, 0.5 h, 0 to 10 deg C, 0.5 h;
DOI:10.1246/cl.1999.687

Reference yield: 90.0%

: 124-63-0
methanesulfonyl chloride

: 122854-68-6
(R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

: 122840-78-2
Methanesulfonic acid (R)-2-cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 5 ℃; for 2h;
DOI:10.1246/cl.1999.687

Reference yield:

: 122854-68-6
(R)-2-Cyclohexyl-1-((3aR,5S,6aR)-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-5-yl)-ethanol

: (S)-2-Cyclohexyl-1-((S)-5-methoxy-tetrahydro-furan-2-yl)-ethylamine

Guidance literature:: Multi-step reaction with 7 steps

1: 90 percent / Et₃N / CH₂Cl₂ / 2 h / 5 °C

2: 97 percent / NaN₃ / dimethylformamide / 40 h / 80 °C

3: 100 percent / cc. H₂SO₄ / 2 h / Ambient temperature

4: 55 percent NaH, imidazole / tetrahydrofuran / 1 h / 5 °C

5: 1 h / 5 °C

6: 61 percent / n-Bu₃SnH, AIBN / toluene / 0.25 h / 100 °C

7: 95 percent / H₂ / 5 percent Pd/C / ethanol / 12 h / 760 Torr / Ambient temperature

With 1H-imidazole; sodium azide; 2,2'-azobis(isobutyronitrile); sulfuric acid; hydrogen; tri-n-butyl-tin hydride; sodium hydride; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1246/cl.1999.687