5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

Base Information

Chemical Name:5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine
CAS No.:267666-00-2
Molecular Formula:C₂₉H₃₈N₂O₆Si
Molecular Weight:538.716
Hs Code.:

Synonyms:5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

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Technology Process of 5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

There total 5 articles about 5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine 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: 58.0%

: 146557-58-6
3-C-allyl-1-[5-O-(tert-butyldiphenylsilyl)-2,3-dideoxy-β-D-erythro-pentofuranosyl]thymine

: 267666-00-2
5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; at 20 ℃; for 3h;
DOI:10.1080/15257770008035014

Reference yield:

: 101527-40-6
5'-O-tert-butyldiphenylsilylthymidine

: 267666-00-2
5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / Et₃N; DMAP / tetrahydrofuran / 3 h / 20 °C

2: 84 percent / AIBN / benzene / 15 h / Heating

3: 58 percent / OsO₄; N-methylmorpholine oxide / acetone; H₂O / 3 h / 20 °C

With dmap; osmium(VIII) oxide; 2,2'-azobis(isobutyronitrile); 4-methylmorpholine N-oxide; triethylamine; In tetrahydrofuran; water; acetone; benzene; 1: Substitution / 2: radical allylation / 3: dihydroxylation;
DOI:10.1080/15257770008035014

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 267666-00-2
5'-O-(tert-butyldiphenylsilyl)-3'-C-(1,2-dihydroxy)propyl-3'-deoxythymidine

Guidance literature:: Multi-step reaction with 4 steps

1: 58 percent / imidazole / dimethylformamide / 0.25 h / 20 °C

2: 80 percent / Et₃N; DMAP / tetrahydrofuran / 3 h / 20 °C

3: 84 percent / AIBN / benzene / 15 h / Heating

4: 58 percent / OsO₄; N-methylmorpholine oxide / acetone; H₂O / 3 h / 20 °C

With 1H-imidazole; dmap; osmium(VIII) oxide; 2,2'-azobis(isobutyronitrile); 4-methylmorpholine N-oxide; triethylamine; In tetrahydrofuran; water; N,N-dimethyl-formamide; acetone; benzene; 1: Substitution / 2: Substitution / 3: radical allylation / 4: dihydroxylation;
DOI:10.1080/15257770008035014