HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 725670Generated: October 30, 2026
4-Hydroxybenzaldehyde → HCID 19708318, compound
https://huagongshe.com/reaction/725670
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 4-[2-(4-Nitrophenyl)diazenyl]benzoic acid | HCID 19708323 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19708318 | HCID 19708318 | 97.6% |
Reaction Steps
0.6 g of N,N'-dicyclohexylcarbodiimide is added at room temperature while stirring to a solution of 1.0 g of 4-(4-nitrophenylazo)benzoic acid, 0.3 g of 4-hydroxybenzaldehyde and 0.04 g of 4-dimethylaminopyridine in 20 ml of dichlormethane. The reaction mixture is stirred at room temperature overnight, poured into 100 ml of water and then extracted three times with 50 ml of dichloromethane each time. The organic phases are combined, washed twice with 100 ml of water each time, dried over magnesium sulphate, filtered and the filtrate is concentrated. Chromatographic purification of the residue on silica gel with hexane/ethyl acetate (vol. 1:1) and two-fold recrystallization from ethanol of the fractions which are pure according to thin-layer chromatography gives 0.9 g of 4-[4-(4-nitrophenylazo)benzoyloxy]benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05707544 |
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| Source dataset | uspto-grants-1998_01 |
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| ORD ID | ord-c7bca4095eff4a4e8a8a851bea63177d |
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| Source note | uspto-grants-1998_01 |
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