Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thymidine | HCID 5789 | — |
| Reactant | 4-Nitrobenzoyl chloride | HCID 8502 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 69967848 | HCID 69967848 | 58% |
Reaction Steps
Thymidine (2.42 g; 10 mmol) is dried by coevaporation in pyridine, then taken up in 200 ml of anhydrous pyridine and cooled to 4° C. p-Nitrobenzoyl chloride (2.04 g; 11 mmol) is added. The temperature is allowed to rise and the reaction is left overnight at room temperature. The reaction is stopped with 5 ml of saturated sodium bicarbonate. The reaction mixture is concentrated and then taken up in 500 ml of chloroform. The organic solution obtained is washed with 2×500 ml of 0.5M NaHCO3 and then with 250 ml of saturated NaCl. The aqueous phases are counter-extracted with 100 ml of CHCl3. The organic phases are evaporated. The pure product is obtained by column chromatography on silica. It is eluted with 5% of methanol in chloroform. Yield=58%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05837859 |
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| Source dataset | uspto-grants-1998_11 |
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| ORD ID | ord-9b58cf7788b34235a64633e0d28afbf9 |
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| Source note | uspto-grants-1998_11 |
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