(2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

Base Information

Chemical Name:(2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone
CAS No.:1431617-88-7
Molecular Formula:C₂₄H₃₀O₂Si
Molecular Weight:378.587
Hs Code.:

Synonyms:(2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

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Chemical Property of (2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

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Technology Process of (2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

There total 7 articles about (2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone 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:

: 1431617-85-4
(2R,3R,4S)-2-[(tert-butyldiphenylsilyl)oxy]-3-methyl-4-pivaloyloxy-cyclohexanone

: 1431617-88-7
(2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.75 h / 0 - 20 °C

1.2: 4 h / -78 - 20 °C

2.1: diisobutylaluminium hydride / dichloromethane; toluene / 1.5 h / -78 - -40 °C / Inert atmosphere

3.1: Dess-Martin periodane / dichloromethane / 1 h / 20 °C / Inert atmosphere

With n-butyllithium; diisobutylaluminium hydride; Dess-Martin periodane; In tetrahydrofuran; hexane; dichloromethane; toluene; 1.2: |Wittig Olefination;

Reference yield:

: 1431137-92-6
(2R,3S,4S)-2-hydroxy-3-methyl-4-pivaloyloxy-cyclohexanone

: 1431617-88-7
(2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: silver nitrate / N,N-dimethyl-formamide / 30 h / 20 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran; hexane / 0.75 h / 0 - 20 °C

2.2: 4 h / -78 - 20 °C

3.1: diisobutylaluminium hydride / dichloromethane; toluene / 1.5 h / -78 - -40 °C / Inert atmosphere

4.1: Dess-Martin periodane / dichloromethane / 1 h / 20 °C / Inert atmosphere

With n-butyllithium; diisobutylaluminium hydride; Dess-Martin periodane; silver nitrate; In tetrahydrofuran; hexane; dichloromethane; N,N-dimethyl-formamide; toluene; 2.2: |Wittig Olefination;

Reference yield:

: 1431617-86-5
(2R,3R,4S)-2-[(tert-butyldiphenylsilyl)oxy]-3-methyl-1-methylene-4-pivaloyloxy-cyclohexane

: 1431617-88-7
(2S,3R)-3-[(tert-butyldiphenylsilyl)oxy]-2-methyl-4-methylene-cyclohexanone

Guidance literature:: Multi-step reaction with 2 steps

1: diisobutylaluminium hydride / dichloromethane; toluene / 1.5 h / -78 - -40 °C / Inert atmosphere

2: Dess-Martin periodane / dichloromethane / 1 h / 20 °C / Inert atmosphere

With diisobutylaluminium hydride; Dess-Martin periodane; In dichloromethane; toluene;