(E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ⁵-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol

Base Information

• Chemical Name: (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ⁵-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol
• CAS No.: 887143-90-0
• Molecular Formula: C₁₇H₂₁O₆P
• Molecular Weight: 352.324
• Mol file: 887143-90-0.mol

Synonyms:(E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ⁵-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol

Chemical Property of (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ⁵-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ⁵-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol

There total 4 articles about (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ⁵-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-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: 72.0%

(1S,6R,8R)-8-Vinyl-2,9,10-trioxa-1-phospha-bicyclo[4.3.1]dec-4-ene 1-oxide (887143-81-9) + (2R)-1-(benzyloxy)but-3-en-2-ol (93553-66-3,109613-59-4,114819-44-2,113426-94-1) → (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ5-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol (887143-90-0)

Guidance literature:

Hoveyda-Grubbs catalyst second generation; In dichloromethane; at 50 ℃;

DOI:10.1021/ol0602809

Reference yield:

(3R,5R)-hepta-1,6-diene-3,5-diol → (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ5-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol (887143-90-0)

Guidance literature:

Multi-step reaction with 4 steps

1: 70 percent / phosphoryl trichloride; Et₃N; DMAP / CH₂Cl₂ / 0.42 h / 0 °C

2: 88 percent / tetrahydrofuran / -40 °C

3: 81 percent / Grubbs second-generation catalyst

4: 72 percent / Hoveyda-Grubbs second-generation catalyst / CH₂Cl₂ / 50 °C

With dmap; triethylamine; trichlorophosphate; tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; Hoveyda-Grubbs catalyst second generation; In tetrahydrofuran; dichloromethane;

DOI:10.1021/ol0602809

Reference yield:

(4R,6R)-2-Chloro-4,6-divinyl-[1,3,2]dioxaphosphinane 2-oxide (887343-97-7) → (E)-(R)-1-Benzyloxy-4-((1R,6R,8R)-1-oxo-2,9,10-trioxa-1λ5-phospha-bicyclo[4.3.1]dec-4-en-8-yl)-but-3-en-2-ol (887143-90-0)

Guidance literature:

Multi-step reaction with 3 steps

1: 88 percent / tetrahydrofuran / -40 °C

2: 81 percent / Grubbs second-generation catalyst

3: 72 percent / Hoveyda-Grubbs second-generation catalyst / CH₂Cl₂ / 50 °C

tricyclohexylphosphine[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidine][benzylidene]ruthenium(II) dichloride; Hoveyda-Grubbs catalyst second generation; In tetrahydrofuran; dichloromethane;

DOI:10.1021/ol0602809

upstream raw materials:

(1S,6R,8R)-8-Vinyl-2,9,10-trioxa-1-phospha-bicyclo[4.3.1]dec-4-ene 1-oxide

(2R)-1-(benzyloxy)but-3-en-2-ol

(4R,6R)-2-Chloro-4,6-divinyl-[1,3,2]dioxaphosphinane 2-oxide

(4R,6R)-2-Allyloxy-4,6-divinyl-[1,3,2]dioxaphosphinane 2-oxide