HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → HCID 14178011, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 11007921 | HCID 11007921 | — |
| Reactant | 4-(5-Nonyl-2-pyrimidinyl)phenol | HCID 135824745 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 14178011 | HCID 14178011 | 37.2% |
Reaction Steps
1.31 g (5 mmol) of triphenyl phosphine and 0.79 g (5 mmol) of diethyl azodicarboxylate are combined in 10 ml of tetrahydrofuran at 0° C. After 20 minutes, 1.49 g (5 mmol) of 2-(4-hydroxyphenyl)-5-n-nonylpyrimidine and 0.72 g (5 mmol) of (2S,3S)-2,3-epoxyoctane, each in 8 ml of tetrahydrofuran, are added. After 24 hours, the mixture is evaporated to dryness in vacuo, and the residue is chromatographed on silica gel (200 g) using CH2Cl2. After recrystallization from hexane, 0.79 g of colorless crystals is obtained; (α) D25 : -15.3° (c=5,CHCl3)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04876028 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-876e505c9b664ba4a18b644c0b95eac4 |
| Source note | uspto-grants-1989_10 |