(3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

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Chemical Name:(3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol
CAS No.:217089-44-6
Molecular Formula:C₂₅H₃₄O₆Si
Molecular Weight:458.627
Hs Code.:

Synonyms:(3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

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Chemical Property of (3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

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Technology Process of (3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

There total 4 articles about (3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol 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: 98.0%

: 4495-04-9
1,2-O-isopropylidene-α-D-allofuranose

: 58479-61-1
tert-butylchlorodiphenylsilane

: 217089-44-6
(3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at -20 ℃; for 2h;
DOI:10.1016/S0040-4020(98)00837-0

Reference yield:

: 14686-89-6
(1,2:5,6)-di-O-isopropylidene-D-gulose

: 217089-44-6
(3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / AcOH / H₂O / 16 h / Ambient temperature

2: 98 percent / imidazole / dimethylformamide / 2 h / -20 °C

With 1H-imidazole; acetic acid; In water; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(98)00837-0

Reference yield:

: 2847-00-9
1,2:5,6-di-O-isopropylidene-α-D-hexofuran-3-ulose

: 217089-44-6
(3aR,5R,6R,6aR)-5-[(R)-2-(tert-Butyl-diphenyl-silanyloxy)-1-hydroxy-ethyl]-2,2-dimethyl-tetrahydro-furo[2,3-d][1,3]dioxol-6-ol

Guidance literature:: Multi-step reaction with 3 steps

1: NaBH₄ / ethanol; H₂O / 1 h / 0 °C

2: 98 percent / AcOH / H₂O / 16 h / Ambient temperature

3: 98 percent / imidazole / dimethylformamide / 2 h / -20 °C

With 1H-imidazole; sodium tetrahydroborate; acetic acid; In ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(98)00837-0