HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Phenoxyacetaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | (2,2-Diethoxyethoxy)benzene | HCID 96328 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Phenoxyacetaldehyde | HCID 75033 | — |
Reaction Steps
0.84 g (4 mmol) of 69A, 5 mL of acetic acid, 2.5 mL of 1N aqueous hydrochloric acid and 20 mL of ethanol were mixed and heated under reflux under an argon atmosphere for 3 hours. Ethanol was evaporated. Then the resulting residue was dispersed in dichloromethane and extracted with saturated sodium bicarbonate solution. The organic phase was dried with sodium sulfate and the solvent evaporated in vacuum. The crude product was obtained in almost quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08389555B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-2ec187ccb9594cdb8a00a7050c53f9f6 |
| Source note | uspto-grants-2013_03 |