HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 1-[4-Benzoyloxy-3-(benzoyloxymethyl)-1-butyl]-5-vinyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracil | HCID 10037283 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 1-[4-Benzoyloxy-3-(benzoyloxymethyl)-1-butyl]-5-vinyluracil | HCID 11091584 | 65.6% |
Reaction Steps
Benzoylchloride (600 mg, 4.2 mmol) was added to a solution of 20 (450 mg, 1.87 mmol) in dry pyridine (50 ml) and the reaction was allowed to proceed at 25° C. with stirring for 48 h. The reaction mixture was poured onto ice water (50 ml) and extracted with dichloromethane (3×50 ml). The dichloromethane extract was dried over sodium sulfate, the solvent was removed in vacuo and the residue obtained was purified by elution from a silica gel column using chloroform-methanol (97:3, v/v) as eluent to yield 22 as a viscous oil (550 mg, 65.4%) which was used directly in the next reaction step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07589077B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-41e1be21bf4a4ce3b5532f1bc5d1a1ff |
| Source note | uspto-grants-2009_09 |