HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634120Generated: November 3, 2026
4-Hydroxybenzaldehyde → HCID 12419541, compound
https://huagongshe.com/reaction/1634120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 12419541 | HCID 12419541 | 126.8% |
Reaction Steps
4-Hydroxybenzaldehyde (20 mmol) was dissolved in absolute EtOH (150 mL) and treated with solid NaOEt (24 mmol). After stirring for 15 minutes, 4-bromobutyronitrile (24 mmol) was added and reaction mixture was heated overnight at 90° C. in an oil bath. After letting the reaction cool to room temperature, volatiles were removed, the residue was taken up in ice, adjusted to pH 6 with 1N sulfuric acid, and extracted with methylene chloride. The organic phase was washed with brine, dried over MgSO4 and concentrated. Chromatography over silica gel (eluant, 5% EtOAc in hexanes) gave the 4-(3-cyanopropoxy)benzaldehyde (4.8 g, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06506747B1 |
|---|
| Source dataset | uspto-grants-2003_01 |
|---|
| ORD ID | ord-37895a13fd5144e387b90ba9c93d9f97 |
|---|
| Source note | uspto-grants-2003_01 |
|---|