HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-(Trimethylsilyl)butyl 4-(5-octyloxypyrimidin-2-yl)-phenyl ether
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-(Trimethylsilyl)butan-1-ol | HCID 262845 | — |
| Reactant | Phenol, 4-[5-(octyloxy)-2-pyrimidinyl]- | HCID 135708811 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(Trimethylsilyl)butyl 4-(5-octyloxypyrimidin-2-yl)-phenyl ether | HCID 14744848 | — |
Reaction Steps
439 mg (3 mmol) of 4-(Trimethylsilyl)butan-1-ol and 901 mg (3 mmol) of 4-(5-n-octyloxypyrimidin-2-yl)phenol are added to the solution of 0.46 ml (3 mmol) of diethyl azodicarboxylate and 790 mg (3 mmol) of triphenylphosphine in 15 ml of dry tetrahydrofuran. After a reaction time of 15 h, the solvent is distilled off and the residue is purified chromatographically (SiO2 /CH2Cl2). After recrystallization from n-hexane, 790 mg of colorless crystals are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05348684 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-0ca4137002b94de5b39231a9fa01d208 |
| Source note | uspto-grants-1994_09 |