HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434718Generated: October 30, 2026
Salicylaldehyde → 4-(2-Hydroxybenzylideneamino)-3,5-dimethylphenol
https://huagongshe.com/reaction/434718
Participants
| Role | Name | HCID | Charge |
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| Reactant | Salicylaldehyde | HCID 6998 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 4-Amino-3,5-dimethylphenol | HCID 76543 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-(2-Hydroxybenzylideneamino)-3,5-dimethylphenol | HCID 135689610 | 82% |
Reaction Steps
To a 500 milliliter round bottom flask equipped with a water condenser, magnetic stirrer and drying tube was added 13.72 grams (0.10 mole) of 4-amino-3,5-dimethylphenol, 12.21 grams (0.10 mole) of salicylaldehyde and 250 milliliters of ethyl acetate. The resulting reaction mixture was then heated to 55° C. and stirred for 19 hours at ambient pressure. After cooling the reaction mixture to room temperature, it was filtered and concentrated under reduced pressure to give a brown oil which solidified on standing. The resulting solidified material was slurried in hexane, collected by filtration and dried to yield 19.66 grams (0.082 moles) of 4-(2-hydroxybenzylideneamino)-3,5-dimethylphenol in the form of a yellow solid having a melting point of 145°-147° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04399148 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-4390cba2efc44e85b57def3af693fd6f |
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| Source note | uspto-grants-1983_08 |
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