HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 3-[4-Chloro-2-(1-methyl-2-propynyloxy)phenyl]-1-methyl-6-trifluoromethyluracil
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Butyn-2-ol | HCID 16239 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-Chloro-2-hydroxyphenyl-1-methyl-6-trifluoromethyluracil | HCID 23289173 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[4-Chloro-2-(1-methyl-2-propynyloxy)phenyl]-1-methyl-6-trifluoromethyluracil | HCID 23289183 | 94.2% |
Reaction Steps
1.7 g (5.3 mmol) of 3-(4-chloro-2-hydroxyphenyl)-1-methyl-6-trifluoromethyluracil, 0.63 g (9.0 mmol) of 1-butyn-3-ol and 1.57 g (6.0 mmol) of triphenylphosphine were dissolved in 100 ml of tetrahydrofuran, and 1.0 g (6.0 mmol) of diethyl azodicarboxylate was dropwise added thereto under cooling with ice. After stirring at room temperature for 1 hour, the solvent was distilled off. Then, the obtained residue was purified by silica gel column chromatography to obtain 1.86 g (yield: 93.9%) of the desired product as white crystals. Melting point: 96-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06130187 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-011bc2d203404f63aea22967a21a57d0 |
| Source note | uspto-grants-2000_10 |