HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thymidine → 5'-O-tert-Butyldimethylsilylthymidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thymidine | HCID 5789 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5'-O-tert-Butyldimethylsilylthymidine | HCID 10251259 | — |
Reaction Steps
A solution of thymidine dT (2.85 g, 11.76 mmol), imidiazole (2.44 g, 35.80 mmol) and TBSCl (1.77 g, 11.76 mmol) in anhydrous CH2Cl2 (20 mL) was stirred at room temperature overnight under a N2 atmosphere. The reaction mixture was then concentrated in vacuo to a viscous oil, followed by the addition of ethyl ether (60 mL) and water (60 mL). The organic layer was separated and washed twice with water (20 mL each), and the combined aqueous layer was extracted with ethyl ether (20 mL). The combined organic layer was dried over Na2SO4, concentrated in vacuo and purified by silica gel column chromatography to give 5′-O-tert-butyldimethylsilyl-thymidine dT.01 (3.44 g, 82%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897737B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-7e6114f3df0e4959a72434e1068ec6e6 |
| Source note | uspto-grants-2011_03 |