HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → HCID 56974686, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | HCID 54142683 | HCID 54142683 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 56974686 | HCID 56974686 | 77% |
Reaction Steps
To a stirred solution of (1R,3S)-3-tetrahydropyranyloxycyclopentanol (2.00 g, 10.7 mmol), phenol (1.20 g, 12.0 mmol) and triphenylphosphine (3.20 g, 12.0 mmol) in dry THF (40 ml) cooled to 0° C. was added dropwise a solution of diethyl azodicarboxylate (2.60 g, 15.0 mmol) in dry THF (10 ml). The mixture was stirred for 1 h at room temperature and then the volatiles removed under reduced pressure. Chromatographic purification of the residue {SiO2, 150 g; hexane/ethyl acetate (20:1)} provided 2.16 g (77 %) of the title compound as a colorless oil: 1H NMR δ7.33-7.22 (m, 2H), 6.99-6.83 (m, 3H), 4.98-4.81 (m, 1H), 4.70-4.60 (m, 1H), 4.55-4.41 (m, 1H), 4.00-3.85 (m, 1H), 3.58-3.47 (m, 1H), 2.30-1.45 (m, 12H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05681858 |
| Source dataset | uspto-grants-1997_10 |
| ORD ID | ord-15b03486f2604da6bb19a199232d595a |
| Source note | uspto-grants-1997_10 |