(+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

Base Information

Chemical Name:(+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol
CAS No.:1333041-65-8
Molecular Formula:C₄₀H₆₀O₅Si
Molecular Weight:648.999
Hs Code.:

Synonyms:(+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

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Chemical Property of (+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

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Technology Process of (+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

There total 13 articles about (+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-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: 100.0%

: 1333041-53-4
(+)-(2R,3R,4S,5S,6S,7S,8S)-methyl 5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonanoate

: 1333041-65-8
(+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

Guidance literature:: (+)-(2R,3R,4S,5S,6S,7S,8S)-methyl 5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonanoate; With diisobutylaluminium hydride; In hexanes; dichloromethane; at -40 ℃; for 1h; Inert atmosphere;

With methanol; In hexanes; dichloromethane; at -40 ℃;
DOI:10.1021/jo2013884

Reference yield:

: 1096707-44-6
methyl (2S,3S,4S)-3,5-bis(benzyloxy)-2,4-dimethylpentanoate

: 1333041-65-8
(+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

Guidance literature:: Multi-step reaction with 11 steps

1.1: diisobutylaluminium hydride / dichloromethane / -40 °C / Inert atmosphere

2.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -78 °C / Inert atmosphere

2.2: -78 °C / Inert atmosphere

3.1: titanium tetrachloride / dichloromethane / 78 °C / Inert atmosphere

4.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / -78 °C / Inert atmosphere

4.2: -78 °C / Inert atmosphere

5.1: trifluorormethanesulfonic acid / dichloromethane; cyclohexane / 0 °C

6.1: diisobutylaluminium hydride / hexanes; dichloromethane / 1 h / -40 °C / Inert atmosphere

6.2: -40 °C

7.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.5 h / -78 °C / Inert atmosphere

7.2: 1 h / -78 °C / Inert atmosphere

8.1: boron trifluoride diethyl etherate / dichloromethane / 1 h / -78 °C / Inert atmosphere

9.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / -78 °C / Inert atmosphere

9.2: -78 °C / Inert atmosphere

10.1: 2,6-dimethylpyridine / dichloromethane / 1.5 h / 0 °C / Inert atmosphere

11.1: diisobutylaluminium hydride / hexanes; dichloromethane / 1 h / -40 °C / Inert atmosphere

11.2: -40 °C

With 2,6-dimethylpyridine; oxalyl dichloride; trifluorormethanesulfonic acid; di-n-butylboryl trifluoromethanesulfonate; boron trifluoride diethyl etherate; titanium tetrachloride; diisobutylaluminium hydride; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In hexanes; dichloromethane; cyclohexane; 2.1: Swern oxidation / 2.2: Swern oxidation / 3.1: Mukaiyama reaction / 7.1: Swern oxidation / 7.2: Swern oxidation / 8.1: Mukaiyama reaction;
DOI:10.1021/jo2013884

Reference yield:

: 1096706-74-9
(2S,3S,4S)-3,5-bis(benzyloxy)-2,4-dimethylpentanal

: 1333041-65-8
(+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol

Guidance literature:: Multi-step reaction with 9 steps

1.1: titanium tetrachloride / dichloromethane / 78 °C / Inert atmosphere

2.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / -78 °C / Inert atmosphere

2.2: -78 °C / Inert atmosphere

3.1: trifluorormethanesulfonic acid / dichloromethane; cyclohexane / 0 °C

4.1: diisobutylaluminium hydride / hexanes; dichloromethane / 1 h / -40 °C / Inert atmosphere

4.2: -40 °C

5.1: oxalyl dichloride; dimethyl sulfoxide / dichloromethane / 0.5 h / -78 °C / Inert atmosphere

5.2: 1 h / -78 °C / Inert atmosphere

6.1: boron trifluoride diethyl etherate / dichloromethane / 1 h / -78 °C / Inert atmosphere

7.1: di-n-butylboryl trifluoromethanesulfonate; N-ethyl-N,N-diisopropylamine / dichloromethane / 1.5 h / -78 °C / Inert atmosphere

7.2: -78 °C / Inert atmosphere

8.1: 2,6-dimethylpyridine / dichloromethane / 1.5 h / 0 °C / Inert atmosphere

9.1: diisobutylaluminium hydride / hexanes; dichloromethane / 1 h / -40 °C / Inert atmosphere

9.2: -40 °C

With 2,6-dimethylpyridine; oxalyl dichloride; trifluorormethanesulfonic acid; di-n-butylboryl trifluoromethanesulfonate; boron trifluoride diethyl etherate; titanium tetrachloride; diisobutylaluminium hydride; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; In hexanes; dichloromethane; cyclohexane; 1.1: Mukaiyama reaction / 5.1: Swern oxidation / 5.2: Swern oxidation / 6.1: Mukaiyama reaction;
DOI:10.1021/jo2013884