1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil

Base Information

• Chemical Name: 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil
• CAS No.: 357610-01-6
• Molecular Formula: C₃₁H₅₀N₂O₇SeSi₃
• Molecular Weight: 725.964
• Mol file: 357610-01-6.mol

Synonyms:1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil

Chemical Property of 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil

There total 4 articles about 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil 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: 97.0%

Chlorodimethylvinylsilane (1719-58-0) + 1-[1-C-Phenylseleno-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil (288103-33-3) → 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil (357610-01-6)

Guidance literature:

With dmap; triethylamine; In toluene; at 20 ℃; for 0.166667h;

DOI:10.1002/1521-3765(20010601)7:11<2332::AID-CHEM23320>3.0.CO;2-W

Reference yield:

Phenylselenyl chloride (5707-04-0) → 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil (357610-01-6)

Guidance literature:

Multi-step reaction with 3 steps

1.1: LiHMDS / tetrahydrofuran / 1 h / -70 °C

1.2: tetrahydrofuran / 1 h / -70 °C

2.1: 90 percent / CeCl₃*7H₂O; NaBH₄ / methanol / 0.17 h / -70 °C

3.1: 97 percent / DMAP; Et₃N / toluene / 0.17 h / 20 °C

With dmap; sodium tetrahydroborate; cerium(III) chloride; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; toluene;

DOI:10.1002/1521-3765(20010601)7:11<2332::AID-CHEM23320>3.0.CO;2-W

Reference yield:

1-((6aR,8R,9aR)-2,2,4,4-tetraisopropyl-9-oxotetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)pyrimidine-2,4(1H,3H)-dione (84828-97-7) → 1-[1-C-Phenylseleno-2-O-dimethylvinylsilyl-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil (357610-01-6)

Guidance literature:

Multi-step reaction with 3 steps

1.1: LiHMDS / tetrahydrofuran / 1 h / -70 °C

1.2: tetrahydrofuran / 1 h / -70 °C

2.1: 90 percent / CeCl₃*7H₂O; NaBH₄ / methanol / 0.17 h / -70 °C

3.1: 97 percent / DMAP; Et₃N / toluene / 0.17 h / 20 °C

With dmap; sodium tetrahydroborate; cerium(III) chloride; triethylamine; lithium hexamethyldisilazane; In tetrahydrofuran; methanol; toluene;

DOI:10.1002/1521-3765(20010601)7:11<2332::AID-CHEM23320>3.0.CO;2-W

upstream raw materials:

Chlorodimethylvinylsilane

1-[1-C-Phenylseleno-3,5-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-β-D-ribo-pentofuranosyl]uracil

Phenylselenyl chloride

1-((6aR,8R,9aR)-2,2,4,4-tetraisopropyl-9-oxotetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)pyrimidine-2,4(1H,3H)-dione

Downstream raw materials:

1-((3aR,3bR,9aR,10aS)-5,5,7,7-Tetraisopropyl-2,2-dimethyl-1-phenylselanylmethyl-hexahydro-3,4,6,8,10-pentaoxa-2,5,7-trisila-cycloocta[a]pentalen-10a-yl)-1H-pyrimidine-2,4-dione