HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038599Generated: October 30, 2026
Water → 1-(4-(2,2-Diethoxyethoxy)phenyl)ethanone
https://huagongshe.com/reaction/1038599
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4'-Hydroxyacetophenone | HCID 7469 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-(2,2-Diethoxyethoxy)phenyl)ethanone | HCID 63629774 | 133.4% |
Reaction Steps
To a solution of 1-(4-hydroxyphenyl)ethanone (1.00 g, 7.34 mmol) in N,N′-dimethylformamide (24 mL), sodium hydride (purity 50%) (380 mg, 8.07 mmol), and bromoacetaldehyde diethyl acetal (1.30 mL, 8.81 mmol) were added under ice-cold conditions and stirred at 120° C. overnight. Under ice-cold conditions, the reaction solution was added water, and extracted with diethylether. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The obtained residue was purified by silica-gel column chromatography (hexane/ethyl acetate), and the title compound (2.47 g (yield >100%)) was obtained as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08551985B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-2026adeb69eb431785efb232f9c20266 |
|---|
| Source note | uspto-grants-2013_10 |
|---|