(4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane

Base Information

• Chemical Name: (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane
• CAS No.: 220156-24-1
• Molecular Formula: C₃₉H₄₇BO₅Si
• Molecular Weight: 634.696
• Mol file: 220156-24-1.mol

Synonyms:(4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane

Chemical Property of (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane

There total 5 articles about (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane 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:

(4R,5R)-4,5-bis(methoxymethyl)-2-(p-methoxyphenyl)-α,α,α',α'-tetraphenyl-1,3-dioxolane (130888-43-6) → (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane (220156-24-1)

Guidance literature:

Multi-step reaction with 3 steps

1.1: 2,3-dichloro-4,5-dicyano-1,4-benzoquinone / CH₂Cl₂; H₂O / 2 h / 20 °C

1.2: LiAlH₄ / diethyl ether / 2 h / 20 °C

2.1: BH₃*SMe₂ / CH₂Cl₂ / 4 h / Heating

3.1: 12 h / 120 °C

With dimethylsulfide borane complex; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In dichloromethane; water; 1.1: Ring cleavage / 1.2: Reduction / 2.1: Cycloaddition / 3.1: Addition;

DOI:10.1021/jo9910278

Reference yield:

(2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butandiol (130874-89-4) → (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane (220156-24-1)

Guidance literature:

Multi-step reaction with 2 steps

1: BH₃*SMe₂ / CH₂Cl₂ / 4 h / Heating

2: 12 h / 120 °C

With dimethylsulfide borane complex; In dichloromethane; 1: Cycloaddition / 2: Addition;

DOI:10.1021/jo9910278

Reference yield:

(4R,5R)-2-((E)-Hept-1-enyl)-4,5-bis-(methoxy-diphenyl-methyl)-[1,3,2]dioxaborolane (199185-03-0) → (4R,5R)-2-[(E)-2-[3-tert-butyl(dimethyl)siloxymethyl]ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane (220156-24-1)

Guidance literature:

Multi-step reaction with 4 steps

1: Pd(OAc)2 / diethyl ether / 0 °C

2: 98 percent / LiAlH₄ / tetrahydrofuran / 1 h / 0 °C

3: BH₃*SMe₂ / CH₂Cl₂ / 4 h / Heating

4: 12 h / 120 °C

With palladium diacetate; lithium aluminium tetrahydride; dimethylsulfide borane complex; In tetrahydrofuran; diethyl ether; dichloromethane; 1: Cycloaddition / 2: Reduction / 3: Cycloaddition / 4: Addition;

DOI:10.1021/jo9910278

upstream raw materials:

tert-Butyldimethyl(prop-2-ynyloxy)silane

(4R,5R)-4,5-Bis-(methoxy-diphenyl-methyl)-[1,3,2]dioxaborolane

(2R,3R)-1,4-dimethoxy-1,1,4,4-tetraphenyl-2,3-butandiol

(4R,5R)-4,5-bis(methoxymethyl)-2-(p-methoxyphenyl)-α,α,α',α'-tetraphenyl-1,3-dioxolane

Downstream raw materials:

(4R,5R,1'R,2'R)-2-[2-(hydroxymethyl)cyclopropyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane

(4R,5R)-2-[(E)-2-{hydroxymethyl}ethenyl]-4,5-bis[methoxy(diphenyl)methyl]-1,3,2-dioxaborolane