HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489388Generated: October 30, 2026
Dimethylformamide → 2-[(4-chlorobenzyl)oxy]benzaldehyde
https://huagongshe.com/reaction/1489388
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-[(4-chlorobenzyl)oxy]benzaldehyde | HCID 693299 | — |
Reaction Steps
Potassium carbonate (33.17 g) and DMF (180 ml) were added to salicylaldehyde (24.42 g), and the mixture was stirred at room temperature for 10 minutes. Then a mixture of 4-chlorobenzyl chloride (33.82 g) and DMF (20 ml) was added at room temperature over 15 minutes, and the mixture was stirred at 60° C. for 3 hours. After completion of the reaction, ether (500 ml) was added, and the mixture was washed with water (400 ml) three times, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give crude 2-(4-chlorobenzyloxy)benzaldehyde. The ethanol (200 ml) and hydroxylamine hydrochloride (27.80 g) was added to the crude product, and the mixture was stirred at 80° C. overnight. After completion of the reaction, water (400 ml) was added, and the mixture was extracted with methylene chloride (200 ml) three times, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting crude product was recrystallized from ethyl acetate/n-hexane to give 2-(4-chlorobenzyloxy)benzaldehyde oxime (32.06 g) as colorless crystals. mp. 122.5°-123.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05677465 |
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| Source dataset | uspto-grants-1997_10 |
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| ORD ID | ord-ea2cf299aa4c4fed8fc8942e7d2686d9 |
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| Source note | uspto-grants-1997_10 |
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