HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → HCID 10155202, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Propoxybenzaldehyde | HCID 79812 | — |
| Reactant | 2',3',4'-Trimethoxyacetophenone | HCID 83810 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 10155202 | HCID 10155202 | 99% |
Reaction Steps
To a stirred solution of 4-propoxybenzaldehyde (0.781 g, 4.8 mmol) and 2,3,4-trimethoxyacetophenone (1.0 g, 4.8 mmol) in methanol (30 ml) was added a 50% w/v solution of aqueous NaOH (7.60 ml, 0.096 mol). The reaction mixture was stirred at room temperature for 24 h. A pale yellow precipitate was isolated and dried under vacuum over night. 1.693 g (86%) of a pale yellow powder was isolated. 1H-NMR (CDCl3) δ 7.60 (d, 1H), 7.5 (m, 1H), 4.4 (d, 1H), 7.3 (d, 1H), 6.8 (m, 1H), 6.7 (d, 1H), 3.9 (t, 2H), 3.9 (s, 3H), 3.9 (s, 3H), 3.9 (s, 3H), 1.75 (m, 2H), 1.0 (t, 3H). 13C-NMR (CDCl3) δ 191.0. Mass Spectrum m/e (M+1) 357. Anal. Calcd. for C21H24O5.H2O: C, 67.44; H, 7.01. Found: C, 67.49; H, 6.93.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112698B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-ceca459e13a44f18ae5d0b279f62c0f4 |
| Source note | uspto-grants-2006_09 |