(2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol

Base Information

• Chemical Name: (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol
• CAS No.: 334968-86-4
• Molecular Formula: C₂₁H₃₈O₃Si
• Molecular Weight: 366.616
• Mol file: 334968-86-4.mol

Synonyms:(2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol

Chemical Property of (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol

There total 3 articles about (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-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:

(2S,3R)-7-Benzyloxy-1-((S)-4-benzyl-2-thioxo-oxazolidin-3-yl)-2-methyl-3-triethylsilanyloxy-heptan-1-one → (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol (334968-86-4)

Guidance literature:

With lithium borohydride; In methanol; diethyl ether;

DOI:10.1021/ol015652m

Reference yield:

triethylsilyl trifluoromethyl sulfonate (79271-56-0) → (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol (334968-86-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 2,6-lutidine

2: LiBH₄ / methanol; diethyl ether

With 2,6-dimethylpyridine; lithium borohydride; In methanol; diethyl ether;

DOI:10.1021/ol015652m

Reference yield:

(2S,3R)-7-Benzyloxy-1-((S)-4-benzyl-2-thioxo-oxazolidin-3-yl)-3-hydroxy-2-methyl-heptan-1-one → (2R,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptan-1-ol (334968-86-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 2,6-lutidine

2: LiBH₄ / methanol; diethyl ether

With 2,6-dimethylpyridine; lithium borohydride; In methanol; diethyl ether;

DOI:10.1021/ol015652m

upstream raw materials:

triethylsilyl trifluoromethyl sulfonate

Downstream raw materials:

(1S,4S,5R,6R)-1,10-Bis-benzyloxy-1-[(2R,3S,4S)-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-3,4-dihydro-2H-pyran-2-yl]-4-hydroxy-5-methyl-6-triethylsilanyloxy-decan-2-one

(2R,4S,5R,6R)-6-(4-Benzyloxy-butyl)-2-{(S)-benzyloxy-[(2R,3S,4S)-4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-3,4-dihydro-2H-pyran-2-yl]-methyl}-2-methoxy-5-methyl-tetrahydro-pyran-4-ol

(2S,3R)-7-Benzyloxy-2-methyl-3-triethylsilanyloxy-heptanal