1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

Base Information

Chemical Name:1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene
CAS No.:1356563-86-4
Molecular Formula:C₂₉H₃₃ClO₂S
Molecular Weight:481.099
Hs Code.:

Synonyms:1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

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Chemical Property of 1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

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Technology Process of 1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

There total 4 articles about 1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene 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: 96.0%

: [(1S,2R,3R)-2-chloro-3-isopropyl-1-(2-phenylethyl)-2-((R)-p-tolylsulfinyl)cyclopropyl]methanol

: 100-39-0
benzyl bromide

: 1356563-86-4
1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

Guidance literature:: With sodium hydride; sodium iodide; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; for 0.5h; Inert atmosphere;
DOI:10.1016/j.tet.2011.11.085

Reference yield:

: 123849-08-1
(-)-(R)-dichloromethyl p-tolyl sulfoxide

: 1356563-86-4
1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

Guidance literature:: Multi-step reaction with 3 steps

1: lithium diisopropyl amide / tetrahydrofuran / -85 - 20 °C / Inert atmosphere

2: sodium tetrahydroborate / Inert atmosphere

3: sodium hydride; sodium iodide / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; sodium hydride; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.tet.2011.11.085

Reference yield:

: 1312031-62-1
(E)-4-methyl-2-(2-phenylethyl)pent-2-enoic acid ethyl ester

: 1356563-86-4
1-{(R)-[(1R,2S,3R)-2-(benzyloxymethyl)-1-chloro-3-isopropyl-2-(2-phenylethyl)cyclopropyl]sulfinyl}-4-methylbenzene

Guidance literature:: Multi-step reaction with 3 steps

1: lithium diisopropyl amide / tetrahydrofuran / -85 - 20 °C / Inert atmosphere

2: sodium tetrahydroborate / Inert atmosphere

3: sodium hydride; sodium iodide / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere

With sodium tetrahydroborate; sodium hydride; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil;
DOI:10.1016/j.tet.2011.11.085