(4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

Base Information

Chemical Name:(4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one
CAS No.:359868-24-9
Molecular Formula:C₄₈H₆₀O₄Si₂
Molecular Weight:757.173
Hs Code.:

Synonyms:(4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

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Chemical Property of (4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

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Technology Process of (4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

There total 5 articles about (4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one 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: 95.0%

: 359868-23-8
(3S,4R,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-ol

: 359868-24-9
(4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

Guidance literature:: With Dess-Martin periodane; In dichloromethane; at 20 ℃; for 2h;
DOI:10.1016/S0040-4039(01)00799-7

Reference yield:

: 96691-92-8
(1R,2R,3r,4S,5S)-3-(benzyloxy)-2,4-dimethyl-8-oxa-bicyclo[3.2.1]oct-6-ene

: 359868-24-9
(4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: (+)-diisopinocampheylborane / 24 h / -23 °C

1.2: 96 percent / NaOH; H₂O₂ / H₂O / 6 h / 20 °C

2.1: PCC / CH₂Cl₂ / 3 h / 20 °C

3.1: m-CPBA; NaHCO₃ / CH₂Cl₂ / 10 h / 20 °C

4.1: 88 percent / LiAlH₄ / tetrahydrofuran / 4 h / 0 - 20 °C

5.1: 83 percent / imidazole / CH₂Cl₂ / 2 h / 0 - 20 °C

6.1: 95 percent / Dess-Martin periodinane / CH₂Cl₂ / 2 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; diisopinocampheylborane; sodium hydrogencarbonate; Dess-Martin periodane; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane; 3.1: Baeyer-Villiger oxidation;
DOI:10.1016/S0040-4039(01)00799-7

Reference yield:

: endo-3-benzyloxy-endo,endo-2,4-dimethyl-8-oxabicyclo[3.2.1]oct-6-one

: 359868-24-9
(4S,5S,6S)-5-Benzyloxy-1,7-bis-(tert-butyl-diphenyl-silanyloxy)-4,6-dimethyl-heptan-3-one

Guidance literature:: Multi-step reaction with 4 steps

1: m-CPBA; NaHCO₃ / CH₂Cl₂ / 10 h / 20 °C

2: 88 percent / LiAlH₄ / tetrahydrofuran / 4 h / 0 - 20 °C

3: 83 percent / imidazole / CH₂Cl₂ / 2 h / 0 - 20 °C

4: 95 percent / Dess-Martin periodinane / CH₂Cl₂ / 2 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; sodium hydrogencarbonate; Dess-Martin periodane; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane; 1: Baeyer-Villiger oxidation;
DOI:10.1016/S0040-4039(01)00799-7