HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ozone → HCID 68814795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ozone | HCID 24823 | — |
| Reactant | Methyl bromoacetate | HCID 60984 | — |
| Reactant | HCID 68815056 | HCID 68815056 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 68814795 | HCID 68814795 | — |
Reaction Steps
The desired product was prepared using a procedure similar to step 1 of example 4. Thus, 4-(1-benzyl-3-methyl-2-phenyl-1H-indol-4-yl)-phenol (0.260 g, 0.668 mmol) was reacted with K2C(O3 (0.120 g, 0.868 mmol) and methyl bromoacetate (0.133 g, 0.868 mmol) in acetone (5 ml) to give the product (0.271 g, 0.587 mmol, 88%) as a viscous oil. 1H NMR (DMSO-d6) δ 1.72 (s, 3H), 3.71 (s, 3H), 4.84 (s, 2H), 5.29 (s, 2H), 6.84 (d, J=7.0 Hz, 1H), 6.88 (d, J=7.2 Hz, 2H), 6.98 (d, J=8.7 Hz, 2H), 7.11 (t, J=7.3 Hz, 1H), 7.16 (t, J=7.2 Hz, 1H), 7.22 (t, J=7.0 Hz, 2H), 7.31-7.35 (m, 5H), 7.41 (t, J=7.2 Hz, 1H), 7.45 (t, J=7.5 Hz, 2H); [ESI(+)], m/z 462 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07582773B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-1f12565e1b15491e895c0666c0ed5f1a |
| Source note | uspto-grants-2009_09 |