(1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

Base Information

Chemical Name:(1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol
CAS No.:688364-77-4
Molecular Formula:C₂₅H₃₆O₂S
Molecular Weight:400.626
Hs Code.:

Synonyms:(1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

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Chemical Property of (1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

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Technology Process of (1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

There total 1 articles about (1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol 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: 92.0%

: 84319-69-7
trans-1-cyclohexyl-3-phenyl-2-propen-1-one

: 71242-58-5
(1S,2R,4R)-(-)-10-mercaptoisoboneol

: 688364-77-4
(1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

Guidance literature:: With dimethylaluminum chloride; In hexane; dichloromethane; at 20 ℃; for 24h;
DOI:10.1016/j.tetasy.2004.01.020

Reference yield:

: 688364-77-4
(1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

: (1S,2R,4R)-1-((1R,3R)-3-Cyclohexyl-3-hydroxy-1-phenyl-propylsulfanylmethyl)-7,7-dimethyl-bicyclo[2.2.1]heptan-2-ol

Guidance literature:: With lithium aluminium tetrahydride; In tetrahydrofuran; at 20 ℃; for 2h;
DOI:10.1016/j.tetasy.2004.01.020

Reference yield:

: 688364-77-4
(1R,3R)-1-cyclohexyl-3-[(1S,4R)-2-oxobornane-10-sulfenyl]-3-phenyl-1-propanol

: (1R,3R)-1-cyclohexyl-3-mercapto-3-phenyl-1-propanol

Guidance literature:: Multi-step reaction with 2 steps

1.1: LiAlH₄ / tetrahydrofuran / 2 h / 20 °C

2.1: BF₃*Et₂O / CH₂Cl₂ / 2.5 h / 20 °C

2.2: 1-dodecanethiol / CH₂Cl₂ / 5.5 h / 20 °C

With lithium aluminium tetrahydride; boron trifluoride diethyl etherate; In tetrahydrofuran; dichloromethane; 2.1: Wagner-Meerwein rearrangement;
DOI:10.1016/j.tetasy.2004.01.020