HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Quinuclidinol, (-)- → (S)-3-(4-phenoxyphenoxy)quinuclidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Quinuclidinol, (-)- | HCID 91404 | — |
| Reactant | 4-Iododiphenyl ether | HCID 520399 | — |
| Product | (S)-3-(4-phenoxyphenoxy)quinuclidine | HCID 11392280 | — |
Reaction Steps
3-(R)-Hydroxy-quinuclidine (the product of Reference Example 1, 152 mg, 1.2 mmol), was treated with 1-iodo-4-phenoxy-benzene (178 mg, 0.6 mmol) according to the procedure of Example 3A to provide the title compound. (80 mg, yield, 45.2%). 1H NMR (MeOH-d4, 300 MHz) δ 1.45–1.58 (m, 1H), 1.64–1.85 (m, 2H), 2.00–2.15 (m, 1H), 2.20–2.30 (m, 1H), 2.70–3.10 (m, 5H), 3.34–3.40 (m, 1H), 4.52 (m, 1H), 6.83–6.98 (m, 6H), 7.03 (tt, J=7.5, 1.0 Hz, 1H), 7.30 (t, J=7.5 Hz, 2H) ppm. MS (D m/z 296 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241773B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-0554bae889d244f68960643e2392bf69 |
| Source note | uspto-grants-2007_07 |