Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Vanillin | HCID 1183 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromomethylnaphthalene | HCID 70320 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 965934 | HCID 965934 | 76.3% |
Reaction Steps
2-(Bromomethyl)naphthalene (1.3 g, 5.9 mmol) was added to a suspension of vanillin (0.60 g, 3.9 mmol) and potassium carbonate (1.6 g, 12 mmol) in acetone (10 mL) and treated according to Procedure 3. The crude product was recrystallised from EtOAc/petrol providing 3-methoxy-4-(naphth-2-ylmethoxy)benzaldehyde (0.87 g, 75%) as a colourless crystalline solid; mp 107-108° C.; δH (400 MHz, CDCl3) 3.97 (s, 3H, OCH3), 5.41 (s, 2H, OCH2), 7.38 (m, 1H, Naphth-H), 7.44 (d, J2,6=1.6 Hz, 1H, H2), 7.48-7.50 (m, 3H, H6, Naphth-H), 7.55 (m, 1H, Naphth-H), 7.83-7.89 (m, 4H, Naphth-H), 9.84 (s, 1H, CHO); δC (100 MHz, CDCl3) 56.3, 71.3 109.7, 112.8, 125.1 126.4, 126.5, 126.6, 126.8, 128.0, 128.2, 128.9, 130.6, 133.4, 133.5, 133.7, 150.4, 153.8, 191.1; vmax 991, 1131, 1263, 1505, 1580, 1672, 2884 cm−1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08765812B2 |
|---|
| Source dataset | uspto-grants-2014_07 |
|---|
| ORD ID | ord-f871a746e2f5428a9d678ea9f7c327a8 |
|---|
| Source note | uspto-grants-2014_07 |
|---|