(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

Base Information

Chemical Name:(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan
CAS No.:881651-51-0
Molecular Formula:C₃₈H₅₅IO₄Si₂
Molecular Weight:758.928
Hs Code.:

(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

Synonyms:(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

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Chemical Property of (2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

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Technology Process of (2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

There total 6 articles about (2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan 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:

: 881651-48-5
(E)-(2S,4R,7S)-8-Benzyloxy-7-methyl-oct-5-ene-1,2,4-triol

: 881651-51-0
(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / N-iodosuccinimide; NaHCO₃ / tetrahydrofuran / 36 h / 0 °C

2: 99 percent / Et₃N; 4-DMAP / CH₂Cl₂ / 0 - 25 °C

3: 100 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / 0 °C

With 2,6-dimethylpyridine; dmap; N-iodo-succinimide; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja054750q

Reference yield:

: 881651-46-3
(E)-(S)-6-Benzyloxy-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-5-methyl-hex-3-en-2-one

: 881651-51-0
(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / LiAlH₄; LiI / diethyl ether / -100 - 0 °C

2: 97 percent / aq. acetic acid / 5 h / 40 °C

3: 70 percent / N-iodosuccinimide; NaHCO₃ / tetrahydrofuran / 36 h / 0 °C

4: 99 percent / Et₃N; 4-DMAP / CH₂Cl₂ / 0 - 25 °C

5: 100 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / 0 °C

With 2,6-dimethylpyridine; dmap; N-iodo-succinimide; lithium aluminium tetrahydride; sodium hydrogencarbonate; acetic acid; triethylamine; lithium iodide; In tetrahydrofuran; diethyl ether; dichloromethane;
DOI:10.1021/ja054750q

Reference yield:

: 881651-47-4
(E)-(2R,5S)-6-Benzyloxy-1-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-5-methyl-hex-3-en-2-ol

: 881651-51-0
(2S,3R,5S)-2-((1S,2R)-3-Benzyloxy-1-iodo-2-methyl-propyl)-3-(tert-butyl-dimethyl-silanyloxy)-5-(tert-butyl-diphenyl-silanyloxymethyl)-tetrahydro-furan

Guidance literature:: Multi-step reaction with 4 steps

1: 97 percent / aq. acetic acid / 5 h / 40 °C

2: 70 percent / N-iodosuccinimide; NaHCO₃ / tetrahydrofuran / 36 h / 0 °C

3: 99 percent / Et₃N; 4-DMAP / CH₂Cl₂ / 0 - 25 °C

4: 100 percent / 2,6-lutidine / CH₂Cl₂ / 0.5 h / 0 °C

With 2,6-dimethylpyridine; dmap; N-iodo-succinimide; sodium hydrogencarbonate; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja054750q