HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde dimethyl acetal → 5-Methyl-2-phenyl-1,3-dioxane-5-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde dimethyl acetal | HCID 62375 | — |
| Reactant | Dimethylolpropionic acid | HCID 78501 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Methyl-2-phenyl-1,3-dioxane-5-carboxylic acid | HCID 704798 | — |
Reaction Steps
Into a round bottom flask was added sequentially 3-hydroxy-2-hydroxymethyl-2-methyl-propionic acid (10.0 g, 74.5 mmol), acetone (75.0 mL), benzaldehyde dimethyl acetal (17.02 g, 111.0 mmol) and para-toluenesulfonic acid monohydrate (0.71 g, 3.7 mmol). The resulting mixture was stirred at ambient temperature for 4 h and then filtered. The filter cake was rinsed with cold acetone and dried under vacuum to give the title compound as a white solid. 1H NMR (CDCl3, 300 MHz) δ (ppm): 7.46-7.48 (m, 2H), 7.34-7.36 (m, 3H), 5.49 (s, 1H), 4.65 (d, J=10.8 Hz, 2H), 3.70 (d, J=11.4 Hz, 2H), 1.11 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09206172B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-ecb735d057e5464cb59af99604eff1f1 |
| Source note | uspto-grants-2015_12 |