(1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

Base Information

Chemical Name:(1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane
CAS No.:633294-23-2
Molecular Formula:C₂₉H₄₄O₃Si₂
Molecular Weight:496.838
Hs Code.:

Synonyms:(1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

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Chemical Property of (1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

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Technology Process of (1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

There total 5 articles about (1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane 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: 94.0%

: 58479-61-1
tert-butylchlorodiphenylsilane

: 633294-18-5
(1R,3R,5R,6S)-5-(tert-butyldimethylsilyloxy)-6-methyl-7-oxabicyclo[4.1.0]heptan-3-ol

: 633294-23-2
(1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 3h;
DOI:10.1055/s-2003-41025

Reference yield:

: 36616-60-1
(1R,4R,6R)-4-isopropenyl-1-methyl-7-oxabicyclo[4.1.0]heptan-2-one

: 633294-23-2
(1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

Guidance literature:: Multi-step reaction with 4 steps

1.1: 100 percent / CeCl₃*7H₂O; NaBH₄ / methanol / 0.25 h / -20 °C

2.1: 94 percent / imidazole / toluene; dimethylformamide / 24 h / 20 °C

3.1: O₃; NaHCO₃ / methanol; CH₂Cl₂ / -78 °C

3.2: Ac₂O; Et₃N; DMAP / methanol; CH₂Cl₂ / 12 h / Heating

3.3: 68 percent / K₂CO₃ / methanol / 2 h / 20 °C

4.1: 94 percent / imidazole / dimethylformamide / 3 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; cerium(III) chloride; sodium hydrogencarbonate; ozone; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene; 1.1: Luche reduction;
DOI:10.1055/s-2003-41025

Reference yield:

: 6485-40-1,2244-16-8
(R)-Carvone

: 633294-23-2
(1S,2R,4R,6R)-2-(tert-butyldimethylsilyloxy)-4-(tert-butyldiphenylsilyloxy)-1-methyl-7-oxabicyclo[4.1.0]heptane

Guidance literature:: Multi-step reaction with 5 steps

1.1: 100 percent / H₂O₂; NaOH / methanol

2.1: 100 percent / CeCl₃*7H₂O; NaBH₄ / methanol / 0.25 h / -20 °C

3.1: 94 percent / imidazole / toluene; dimethylformamide / 24 h / 20 °C

4.1: O₃; NaHCO₃ / methanol; CH₂Cl₂ / -78 °C

4.2: Ac₂O; Et₃N; DMAP / methanol; CH₂Cl₂ / 12 h / Heating

4.3: 68 percent / K₂CO₃ / methanol / 2 h / 20 °C

5.1: 94 percent / imidazole / dimethylformamide / 3 h / 20 °C

With 1H-imidazole; sodium hydroxide; sodium tetrahydroborate; cerium(III) chloride; dihydrogen peroxide; sodium hydrogencarbonate; ozone; In methanol; dichloromethane; N,N-dimethyl-formamide; toluene; 2.1: Luche reduction;
DOI:10.1055/s-2003-41025