HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76959Generated: October 29, 2026
Imidazole → 5'-O-tert-butyldimethylsilyloxy-3'-deoxythymidine
https://huagongshe.com/reaction/76959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 2',3'-Dideoxythymidine | HCID 65119 | — |
| Product | 5'-O-tert-butyldimethylsilyloxy-3'-deoxythymidine | HCID 87364841 | 87% |
Reaction Steps
To a stirred solution of 3′-deoxythymidine (2.0 g, 8.84 mmol) in anhydrous DMF (15 mL) were added imidazole (0.90 g, 13.26 mmol) and tert-butyldimethylsilyl chloride (TBDMSCl) (1.73 g, 11.49 mmol) at r.t., followed by stirring for 4 h. After evaporating the solvent, the residue was partitioned between CH2Cl2 and water. The organic layer was dried over Na2SO4 and evaporated to dryness. The organic residue was purified by silica gel column chromatography with MeOH/CH2Cl2 (0-3%) to give the corresponding product (2.60 g, 7.63 mmol, 87%). 1H NMR (CDCl3, 300 MHz) δ 8.80 (br s, 1H, NH), 7.57 (q, 1H, H6, J=1.2 Hz), 6.07 (dd, 1H, H1′, J=4.8 and 6.3 Hz), 4.10-4.18 (m, 1H, H4′), 3.98 (dd, 1H, H5′, J=2.4 and 11.4 Hz), 3.70 (dd, 1H, H5′, J=3.0 and 11.4 Hz), 2.30-2.4 (m, 1H, H2′), 1.93-2.04 (m, 3H, H2′, and 2H3′), 1.91 (d, 9H, 3 CH3), 0.10 (2 s, 6H, 2 CH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835625B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-5a67c9f2df974cbbaf4f429c58cc43c4 |
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| Source note | uspto-grants-2014_09 |
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