HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Ethyl-2-p-ethoxyphenyl-3-hydroxypropionate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Ethyl 4-ethoxyphenylacetate | HCID 181675 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl-2-p-ethoxyphenyl-3-hydroxypropionate | HCID 54407388 | — |
Reaction Steps
Sodium ethoxide solution in ethanol (0.5 M, 18 ml) was added to a solution of ethyl-p-ethoxyphenylacetate (30 g) in dry dimethyl sulphoxide (180 ml) under argon cover. The mixture was stirred for 5 minutes and dry paraformaldehyde (5.4 g) added. After 19 h stirring, acetic acid (1.5 ml) was added, the solution quenched in ice and extracted with ether. The ether layer was washed with sodium bicarbonate solution and water, dried over anhydrous sodium sulphate, and the solvent evaporated. The resulting oil crystallized from petroleum ether (40°-60°) to yield 27.8 g product m.p. 35°-36° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220591 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-1d47db06161c4a72ad1fd939bab6786a |
| Source note | uspto-grants-1980_09 |