HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 1-(3-Hydroxymethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-uracil | HCID 289650 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Hydroxymethyl-4-trityloxybutyl)-1H-pyrimidine-2,4-dione | HCID 59463757 | 34% |
Reaction Steps
To a solution of compound 35 (45 g, 0.213 mol) in dry DMF (225 mL) was added triethylamine (60 mL, 0.425 mol) and stirred at RT for 15 min. The above reaction mixture was cooled to 0° C., added tritylchloride (59 g, 0.213 mol) followed by addition of catalytic amount of 4-DMAP (app. 20 mg) and allowed to stir at RT for 24 h. The reaction was diluted with water (100 mL), extracted with ethyl acetate (5×200 mL), dried and concentrated under vacuum. The crude was purified by column chromatography over silica gel (6% methanol in chloroform) to give the title compound (33 g, 34%). TLC: Chloroform/Methanol, 9:1, Rf=0.5
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08017620B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-75d5b72615494185a9fc19bf77a10d0d |
| Source note | uspto-grants-2011_09 |