HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260709Generated: October 26, 2026
Sodium hydride → 4-[2-(N-Benzoyl-N-methylamino)ethoxy]benzaldehyde
https://huagongshe.com/reaction/2260709
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | N-(2-hydroxyethyl)-N-methylbenzamide | HCID 4047264 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[2-(N-Benzoyl-N-methylamino)ethoxy]benzaldehyde | HCID 18998892 | — |
Reaction Steps
Sodium hydride (60% dispersion in oil, 1.30 g) was added portionwise to a solution of 2-(N-benzoyl-N-methylamino)ethanol (5.0 g) in dry dimethylformamide (100 ml) at room temperature under a nitrogen atmosphere. The mixture was stirred at room temperature for 1 hour prior to the addition of 4-fluorobenzaldehyde (5.09 g, 4.4 ml), and the mixture then heated at 80° C. for 15 hours. The solvent was evaporated and the residue dissolved in water (500 ml) and extracted with ethyl acetate (3×500 ml). The combined ethyl acetate layers were washed with water (2×300 ml), brine (300 ml), dried (MgSO4) and evaporated to yield an oil. The oil was triturated with hexane, and the residue chromatographed on silica gel with 1.5% methanol in dichloromethane to afford the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05478851 |
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| Source dataset | uspto-grants-1995_12 |
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| ORD ID | ord-db686fe8ffe24339a2419a14a7183478 |
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| Source note | uspto-grants-1995_12 |
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