1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

Base Information

Chemical Name:1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil
CAS No.:119932-73-9
Molecular Formula:C₃₅H₄₄N₂O₆Si
Molecular Weight:616.83
Hs Code.:

Synonyms:1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

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Chemical Property of 1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

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Technology Process of 1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

There total 4 articles about 1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>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: 88.0%

: 119932-72-8
1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-1-chloro-3-oxa-2(R)-pentyl>uracil

: 119932-73-9
1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; for 3h; Heating;
DOI:10.1007/BF00475606

Reference yield:

: 119932-71-7
1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-1-hydroxy-3-oxa-2(R)-pentyl>uracil

: 119932-73-9
1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

Guidance literature:: Multi-step reaction with 2 steps

1: 46 percent / Ph₃P, CCl₄ / pyridine / 16 h / 20 °C

2: 88 percent / tributyltin hydride, α,α-azobisisobutyronitril / toluene / 3 h / Heating

With tetrachloromethane; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; triphenylphosphine; In pyridine; toluene;
DOI:10.1007/BF00475606

Reference yield:

: 98807-14-8,119932-68-2
1-((R)-2-Hydroxy-1-{(R)-1-hydroxymethyl-2-[(4-methoxy-phenyl)-diphenyl-methoxy]-ethoxy}-ethyl)-1H-pyrimidine-2,4-dione

: 119932-73-9
1-<4(R)-tert-butyldimethylsilyloxymethyl-5-(p-monomethoxytrityloxy)-3-oxa-2(R)-pentyl>uracil

Guidance literature:: Multi-step reaction with 3 steps

1: 28 percent / imidazole, / pyridine / 16 h / 20 °C

2: 46 percent / Ph₃P, CCl₄ / pyridine / 16 h / 20 °C

3: 88 percent / tributyltin hydride, α,α-azobisisobutyronitril / toluene / 3 h / Heating

With 1H-imidazole; tetrachloromethane; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; triphenylphosphine; In pyridine; toluene;
DOI:10.1007/BF00475606