HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → HCID 9835935, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Dibutyltin dichloride | HCID 12688 | — |
| Reactant | Phenylsilane | HCID 12752 | — |
| Reactant | 4-[4-(1H-Imidazol-1-yl)phenoxy]piperidine | HCID 22036910 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9835935 | HCID 9835935 | — |
Reaction Steps
A solution of the product of Example 6 (130 mg), cyclohexanone (0.06 mL), and dibutyltin dichloride (3 mg) in THF (0.1 mL) was treated with phenylsilane (0.07 mL). After 16 h, the resulting mixture was chromatographed (0–8% 2M methanolic ammonia/DCM), giving the title compound as a waxy solid (18 mg). 1H NMR (400 MHz, CDCl3): 7.75 (t, J=1.2 Hz, 1H), 7.28 (d, J=9.0 Hz, 2H), 7.20 (t, J=1.4 Hz, 1H), 7.18 (t, J=1.2 Hz, 1H), 6.99 (d, J=8.8 Hz, 2H), 4.35–4.27 (m, 1H), 2.76–2.67 (m, 2H), 2.26–2.18 (m, 2H), 2.10 (d, J=7.24 Hz, 2H), 2.05–1.96 (m, 2H), 1.87–1.73 (m, 3H), 0.90 (d, J=6.5 Hz, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07241778B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-5b5096f4e23341858a9b25a2b7ad8fda |
| Source note | uspto-grants-2007_07 |