HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2-Dimethoxypropane → 2,2,5-trimethyl-1,3-dioxane-5-carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Dimethylolpropionic acid | HCID 78501 | — |
| Catalyst | Sodium Bicarbonate | HCID 516892 | — |
| Catalyst | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,2,5-trimethyl-1,3-dioxane-5-carboxylic Acid | HCID 11355776 | 90.4% |
Reaction Steps
To a mixture of 3-hydroxy-2-hydroxymethyl-2-methylpropionic acid (6.71 g, 50 mmol), dimethoxypropane (7.99 mL, 65 mmol) and acetone (50 mL), p-toluenesulfonic acid hydrate (0.048 g, 0.25 mmol) was added and the resulting mixture was stirred at room temperature for 2.5 hours. After the reaction was completed, sodium bicarbonate (0.1 g) was added to the reaction mixture, and the resulting mixture was stirred at room temperature for 5 minutes and concentrated in vacuo. To the resulting residue was added water and the resulting mixture was extracted with ethyl ether. The extract was dried over anhydrous sodium sulphate and concentrated in vacuo to give 2,2,5-trimethyl-1,3-dioxane5-carboxylic acid (7.87 g, yield: 90%) as colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575197B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-cf0d419b82464c6abce57f4ef5fa3653 |
| Source note | uspto-grants-2013_11 |