(4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol

Base Information

• Chemical Name: (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol
• CAS No.: 861821-98-9
• Molecular Formula: C₂₃H₄₂O₄Si
• Molecular Weight: 410.67
• Mol file: 861821-98-9.mol

Synonyms:(4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol

Chemical Property of (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol

There total 4 articles about (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-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: 77.0%

ethyl (4S,5R,6S)-7-(4-methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptanoate (871236-53-2) → (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol (861821-98-9)

Guidance literature:

With diisobutylaluminium hydride; In hexane; dichloromethane; at -78 ℃; for 1h;

DOI:10.1021/jm061385k

Reference yield:

ethyl (4S,5R,6S,2E)-7-(4-methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylhept-2-enoate (861821-97-8) → (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol (861821-98-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 97 percent / NaBH₄ / NiCl₂ / methanol; H₂O; tetrahydrofuran / 1 h / 0 °C

2: 77 percent / DIBALH / hexane; CH₂Cl₂ / 1 h / -78 °C

With sodium tetrahydroborate; diisobutylaluminium hydride; nickel dichloride; In tetrahydrofuran; methanol; hexane; dichloromethane; water;

DOI:10.1021/jm061385k

Reference yield:

(-)-(2S,3R,4S)-3-((tert-butyldimethylsilyl)oxy)-5-((4-methoxybenzyl)oxy)-2,4-dimethylpentan-1-ol (792911-22-9) → (4S,5R,6S)-7-(methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptan-1-ol (861821-98-9)

Guidance literature:

Multi-step reaction with 4 steps

1: Py*SO₃; Et₃N / dimethylsulfoxide

2: NaH / tetrahydrofuran

3: NiCl₂; NaBH₄

4: DIBAL-H

With sodium tetrahydroborate; sulfur trioxide pyridine complex; sodium hydride; diisobutylaluminium hydride; triethylamine; nickel dichloride; In tetrahydrofuran; dimethyl sulfoxide; 2: Horner-Wadsworth-Emmons reaction;

DOI:10.1021/ol050808u

upstream raw materials:

ethyl (4S,5R,6S)-7-(4-methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylheptanoate

ethyl (4S,5R,6S,2E)-7-(4-methoxybenzyloxy)-5-(tert-butyldimethylsilyloxy)-4,6-dimethylhept-2-enoate

(-)-(2S,3R,4S)-3-((tert-butyldimethylsilyl)oxy)-5-((4-methoxybenzyl)oxy)-2,4-dimethylpentan-1-ol

2,4-dideoxy-3-O-[(1,1-dimethylethyl)dimethylsilyl]-5-O-[(4-methoxyphenyl)-methyl]-2,4-dimethyl-L-arabinose

Downstream raw materials:

(4R,5S,10S,11R,12S,E)-5,11,15-tris(tert-butyldimethylsilyloxy)-4,10,12-trimethyl-1-trityloxypentadec-2-en-8-yn-7-one

(4R,5S,7S,10S,11R,12S,E)-5,11,15-tris(tert-butyldimethylsilyloxy)-4,10,12-trimethyl-1-(trityloxy)pentadec-2-en-8-yn-7-ol

(2E,4R,5S,7S,8Z,10S,11R,12S)-5,11,15-tris(tert-butyldimethylsilyloxy)-4,10,12-trimethyl-1-(trityloxy)pentadeca-2,8-dien-7-ol

(4S,5R,6S,7Z,9S,11S,12R,13E)-5,9,11-tris(tert-butyldimethylsilyloxy)-4,6,12-trimethyl-15-(trityloxy)pentadeca-7,13-dien-1-ol