HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227147Generated: October 30, 2026
2,4-Dihydroxybenzaldehyde → HCID 136343263, compound
https://huagongshe.com/reaction/2227147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dihydroxybenzaldehyde | HCID 7213 | — |
| Reactant | HCID 135581365 | HCID 135581365 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136343263 | HCID 136343263 | — |
Reaction Steps
To a suspension of 2.5 g (8.64 mmol) of (R,R)-N-mono[4-(diethylamino)salicylidene]-1,2-cyclohexanediamine in 200 ml of ethanol is added dropwise at room temperature over the course of 45 minutes a solution of 1.19 g (8.64 mmol) of 2,4-dihydroxybenzaldehyde. The suspension is heated at 60° C. for 4 h. After cooling to room temperature the resultant brownish orange solution is concentrated to dryness. The crude product (3.5 g) is resolved by column chromatography (ethyl acetate/methanol 9:1). Yield: 570 mg (16%), yellowish orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06413926B2 |
|---|
| Source dataset | uspto-grants-2002_07 |
|---|
| ORD ID | ord-ff0902ba1c584dd5afa619b784c5fd99 |
|---|
| Source note | uspto-grants-2002_07 |
|---|