HuagongsheHuagongshe Chemistry Print Report · For research reference only
3',4',5'-Trimethoxyacetophenone → HCID 6212878, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3',4',5'-Trimethoxyacetophenone | HCID 14345 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Propoxybenzaldehyde | HCID 79812 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 6212878 | HCID 6212878 | 27% |
Reaction Steps
To a stirred solution of 4-propoxybenzaldehyde (1.5 ml, 9.5 mmol) and 3,4,5-trimethoxyacetophenone (2.0 g, 9.5 mmol) in methanol (30 ml) was added 50% w/v of aqueous sodium hydroxide (7.6 ml, 0.095 mol). The reaction was stirred for 24 h at room temperature. A precipitate was isolated by filtration, washed with pet:ether and subsequently recrystallised from ethanol to give 0.9 g (27%) of a pale yellow powder. 1H-NMR (CDCl3) δ 7.8 (d, 1H), 7.6 (d, 2H), 7.3 (d, 1H), 7.2 (m, 1H), 6.8 (d, 2H), 3.95 (m, 2H), 3.9 (s×2, 9H), 1.8 (t, 2H), 1.0 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112698B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-1d9e9251f889489f8f205e420e8713fd |
| Source note | uspto-grants-2006_09 |