(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

Base Information

Chemical Name:(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol
CAS No.:833481-23-5
Molecular Formula:C₁₉H₃₂O₆Si
Molecular Weight:384.545
Hs Code.:

Synonyms:(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

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Chemical Property of (S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

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Technology Process of (S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

There total 5 articles about (S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol 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:

: 1464-44-4
phenyl-β-D-glucopyranoside

: 833481-23-5
(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

Guidance literature:: Multi-step reaction with 7 steps

1.1: 67 percent / CSA / acetonitrile / 21 h / 20 °C

2.1: 90 percent / BH₃*THF; Bu₂BOTf / 7 h / 0 °C

3.1: 99 percent / NaIO₄ / tetrahydrofuran; H₂O / 15 h / 20 °C

4.1: Et₃N; AcCl; DMAP

4.2: 57 percent / NaBH₄

5.1: 88 percent / imidazole

6.1: NaH / dimethylformamide / 0.5 h / 0 °C

7.1: 66 percent / H₂ / Pd(OH)2 / methanol

With 1H-imidazole; dmap; sodium periodate; borane-THF; di-n-butylboryl trifluoromethanesulfonate; camphor-10-sulfonic acid; hydrogen; sodium hydride; triethylamine; acetyl chloride; palladium dihydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.tetlet.2004.11.057

Reference yield:

: 22887-10-1,42821-94-3,54502-82-8,57783-84-3,61169-05-9,61169-06-0,61221-61-2,75829-66-2,111137-95-2,117677-62-0
phenyl 4,6-O-benzylidene-β-D-glucopyranoside

: 833481-23-5
(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

Guidance literature:: Multi-step reaction with 6 steps

1.1: 90 percent / BH₃*THF; Bu₂BOTf / 7 h / 0 °C

2.1: 99 percent / NaIO₄ / tetrahydrofuran; H₂O / 15 h / 20 °C

3.1: Et₃N; AcCl; DMAP

3.2: 57 percent / NaBH₄

4.1: 88 percent / imidazole

5.1: NaH / dimethylformamide / 0.5 h / 0 °C

6.1: 66 percent / H₂ / Pd(OH)2 / methanol

With 1H-imidazole; dmap; sodium periodate; borane-THF; di-n-butylboryl trifluoromethanesulfonate; hydrogen; sodium hydride; triethylamine; acetyl chloride; palladium dihydroxide; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2004.11.057

Reference yield:

: 833481-17-7
(R)-Benzyloxy-((2R,6S)-5-hydroxy-6-phenoxy-[1,4]dioxan-2-yl)-acetaldehyde

: 833481-23-5
(S)-2-(tert-Butyl-dimethyl-silanyloxy)-1-((2R,5R,6S)-5-methoxy-6-phenoxy-[1,4]dioxan-2-yl)-ethanol

Guidance literature:: Multi-step reaction with 4 steps

1.1: Et₃N; AcCl; DMAP

1.2: 57 percent / NaBH₄

2.1: 88 percent / imidazole

3.1: NaH / dimethylformamide / 0.5 h / 0 °C

4.1: 66 percent / H₂ / Pd(OH)2 / methanol

With 1H-imidazole; dmap; hydrogen; sodium hydride; triethylamine; acetyl chloride; palladium dihydroxide; In methanol; N,N-dimethyl-formamide;
DOI:10.1016/j.tetlet.2004.11.057