HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101779Generated: October 30, 2026
4-Hydroxybenzaldehyde → 5-(4-Hydroxybenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione
https://huagongshe.com/reaction/2101779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(4-Hydroxybenzylidene)-2,2-dimethyl-1,3-dioxane-4,6-dione | HCID 370541 | 94% |
Reaction Steps
Condensation with Meldrum's acid was carried out according to the method of Bigi et. al. Tet. Lett. 2001, 42, 5203-5205. A 2 L pear-shaped flask was charged with 4-hydroxybenzaldehyde (50 g, 409 mmol) (commercially available from Aldrich) and water (400 mL). The flask was placed in a water bath at 75° C. and Meldrum's acid (62 g, 430 mmol) (commercially available from Aldrich) was added as a slurry in water (400 mL). The reaction mixture was agitated for 2 hours and then cooled in an ice bath for 2 hours. The product was collected by filtration and rinsed with cold water. After drying thoroughly, 95 g (94%) of adduct 21.1 was obtained as a fine yellow powder. 1H NMR (500 MHz) (DMSO-d6) δ 9.75 (br s, 1H); 8.27 (s, 1H); 8.24 (d, 2H, J=10 Hz); 6.98 (d, 2H, J=10 Hz), 1.76 (s, 6H). MS ESI (pos.) m/e: 519.0 (2M+Na).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07572934B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-2ae6a4a9c31043198723a9e28fb2df49 |
|---|
| Source note | uspto-grants-2009_08 |
|---|