HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906313Generated: October 29, 2026
Dimethylformamide → 2-Benzyloxy-3-(dimethylamino)acrolein
https://huagongshe.com/reaction/906313
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Benzyloxyacetaldehyde diethyl acetal | HCID 4321487 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Benzyloxy-3-(dimethylamino)acrolein | HCID 54521002 | 53.3% |
Reaction Steps
[(2,2-Diethoxyethoxy)methyl]benzene (8.30 g, 37.0 mmol) stirred under ice cooling was added with phosphorus pentachloride (8.09 g, 38.8 mmol) over 15 minutes. The mixture was stirred at the same temperature for 15 minutes, and then heated and stirred on an oil bath at 75° C. for 75 minutes. The reaction mixture was cooled by stirring at room temperature for 20 minutes, cooled, and then added with anhydrous N,N-dimethylformamide (8.6 mL, 111 mmol) at the same temperature, and the mixture was stirred at room temperature for 3 days. The reaction mixture was added with 8 M aqueous sodium hydroxide on an ice bath until pH became 8 or higher, and then the mixture was diluted with water, and extracted with ether. The organic layer was washed successively with water and saturated brine, dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane:acetone=4:1→2:1) to obtain 2-(benzyloxy)-3-(dimethylamino)acrylaldehyde (4.05 g, 53%) as brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012989B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a987dcb53ad8435b833b2a0771b654eb |
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| Source note | uspto-grants-2011_09 |
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