(3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

Base Information

Chemical Name:(3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane
CAS No.:203392-62-5
Molecular Formula:C₂₇H₄₂O₄S
Molecular Weight:462.694
Hs Code.:

Synonyms:(3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

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Chemical Property of (3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

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Technology Process of (3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

There total 12 articles about (3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane 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: 72.0%

: (3R)-3-[(1R,5S,7aR)-5-hydroxy-7a-methyl-4-(phenylsulfonyl)-2,3,5,6,7,7a-hexahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]-4-tosyloxybutane

: 203392-62-5
(3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

Guidance literature:: (3R)-3-[(1R,5S,7aR)-5-hydroxy-7a-methyl-4-(phenylsulfonyl)-2,3,5,6,7,7a-hexahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]-4-tosyloxybutane; With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 2h;

With lithium aluminium tetrahydride; In tetrahydrofuran; for 0.333333h; Further stages.; Heating;
DOI:10.1002/ejoc.200300611

Reference yield: 36.0%

: 203392-60-3
S-tert-butyl (2R)-2-[(1R,7aR)-7a-methyl-5-oxo-4-phenylthio-2,3,5,6,7,7a-hexahydro-1H-inden-1-yl]-4-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butanethioate

: 203392-62-5
(3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

: (3S,6R)-3-isopropoxy-2-methyl-6-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]heptan-2-ol

Guidance literature:: Multistep reaction.;
DOI:10.1002/ejoc.200300611

Reference yield:

: 203392-58-9
S-tert-butyl (2R)-[(1R,2R)-3-oxo-2-(3-oxo-4-phenylthiobutyl)cyclopentyl]-4-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butanethioate

: 203392-62-5
(3R)-3-[(1R,3aR,4R,7aR)-7a-methyl-4-(phenylsulfonyl)octahydro-1H-inden-1-yl]-1-[(4S)-2,2,5,5-tetramethyl-1,3-dioxolan-4-yl]butane

Guidance literature:: Multi-step reaction with 2 steps

1: 84 percent / KOH / methanol / 1 h / 20 °C

With potassium hydroxide; In methanol;
DOI:10.1002/ejoc.200300611