3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione

Base Information

• Chemical Name: 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione
• CAS No.: 163889-36-9
• Molecular Formula: C₃₀H₄₆N₂O₈Si₂
• Molecular Weight: 618.875
• Mol file: 163889-36-9.mol

Synonyms:3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione

Chemical Property of 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione

There total 3 articles about 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione 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:

Di-tert-butyldichlorosilane (18395-90-9) → 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione (163889-36-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / AgNO₃ / dimethylformamide

2: 1.) t-BuMgCl; 2.) Bu₄NI / 1.) THF, r.t., 5 min; 2.) THF, r.t.

With tert-butylmagnesium chloride; tetra-(n-butyl)ammonium iodide; silver nitrate; In N,N-dimethyl-formamide;

DOI:10.1016/0040-4039(95)00130-5

Reference yield:

N3-benzoyluridine (86988-30-9) → 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione (163889-36-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / AgNO₃ / dimethylformamide

2: 1.) t-BuMgCl; 2.) Bu₄NI / 1.) THF, r.t., 5 min; 2.) THF, r.t.

With tert-butylmagnesium chloride; tetra-(n-butyl)ammonium iodide; silver nitrate; In N,N-dimethyl-formamide;

DOI:10.1016/0040-4039(95)00130-5

Reference yield:

(2-trimethylethylsilylethoxy)methyl chloride (76513-69-4) + N3-benzoyl-3',5'-O-(di-tert-butylsilanediyl)uridine (163889-34-7) → 3-Benzoyl-1-[(4aR,6R,7R,7aR)-2,2-di-tert-butyl-7-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furo[3,2-d][1,3,2]dioxasilin-6-yl]-1H-pyrimidine-2,4-dione (163889-36-9)

Guidance literature:

With tert-butylmagnesium chloride; tetra-(n-butyl)ammonium iodide; Yield given. Multistep reaction; 1.) THF, r.t., 5 min; 2.) THF, r.t.;

DOI:10.1016/0040-4039(95)00130-5

upstream raw materials:

(2-trimethylethylsilylethoxy)methyl chloride

N³-benzoyl-3',5'-O-(di-tert-butylsilanediyl)uridine

Di-tert-butyldichlorosilane

N³-benzoyluridine

Downstream raw materials:

3-Benzoyl-1-[(2R,3R,4R,5R)-4-hydroxy-5-hydroxymethyl-3-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dione

3-Benzoyl-1-[(2R,3R,4R,5R)-5-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-3-(2-trimethylsilanyl-ethoxymethoxy)-tetrahydro-furan-2-yl]-1H-pyrimidine-2,4-dione