(3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene

Base Information

• Chemical Name: (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene
• CAS No.: 114114-17-9
• Molecular Formula: C₂₁H₃₆O₂Si
• Molecular Weight: 348.601
• Mol file: 114114-17-9.mol

Synonyms:(3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene

Chemical Property of (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene

There total 10 articles about (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene 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:

(2R,4R)-4-Benzyloxy-2,4-dimethyl-hex-5-en-1-ol (134744-30-2) + tert-butyldimethylsilyl chloride (18162-48-6) → (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene (114114-17-9)

Guidance literature:

With 1H-imidazole; In N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)96400-1

Reference yield:

(2R,4R)-4-Benzyloxy-2,4-dimethyl-hex-5-enal (114114-16-8) → (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene (114114-17-9)

Guidance literature:

Multi-step reaction with 2 steps

1: LiAlH₄ / diethyl ether

2: ImH / dimethylformamide

With 1H-imidazole; lithium aluminium tetrahydride; In diethyl ether; N,N-dimethyl-formamide;

DOI:10.1016/S0040-4039(00)96400-1

Reference yield:

(2S,3R,5R)-3-Benzyloxy-2-bromomethyl-6-methoxy-3,5-dimethyl-tetrahydro-pyran (134744-29-9,134780-34-0) → (3R,5R)-3-benzyloxy-6-tert-butyldimethylsiloxy-3,5-dimethylhex-1-ene (114114-17-9)

Guidance literature:

Multi-step reaction with 3 steps

1: 80 percent / Zn / H₂O; propan-2-ol / Heating

2: LiAlH₄ / diethyl ether

3: ImH / dimethylformamide

With 1H-imidazole; lithium aluminium tetrahydride; zinc; In diethyl ether; water; N,N-dimethyl-formamide; isopropyl alcohol;

DOI:10.1016/S0040-4039(00)96400-1

upstream raw materials:

(2R,4R)-4-Benzyloxy-2,4-dimethyl-hex-5-en-1-ol

tert-butyldimethylsilyl chloride

(2R,4R)-4-Benzyloxy-2,4-dimethyl-hex-5-enal

1,6-anhydro-2,3-didesoxy-2,4-di-C-methyl-4-O-benzyl-β-D-galactopyranose

Downstream raw materials:

(2R,4R)-2-benzyloxy-5-tert-butyldimethylsiloxy-2,4-dimethylpentanal

(3S,4R,5S,6R,7R,9R)-7-Benzyloxy-10-(tert-butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-3,5,7,9-tetramethyl-dec-1-en-4-ol

(2R,3R,5R,6R)-3-Benzyloxy-6-methoxy-3,5-dimethyl-2-((R)-1-methyl-allyl)-tetrahydro-pyran

(2R,3R,5R,6R)-3-Benzyloxy-6-methoxy-3,5-dimethyl-2-((S)-1-methyl-allyl)-tetrahydro-pyran