HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380964Generated: October 30, 2026
4-Cyanobenzaldehyde → HCID 67130691, compound
https://huagongshe.com/reaction/2380964
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (4-Aminophenyl)(4-phenylpiperazin-1-yl)methanone | HCID 12932882 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67130691 | HCID 67130691 | — |
Reaction Steps
To a stirred solution of (4-amino-phenyl)-(4-phenyl-piperazin-1-yl)-methanone (0.5 g, 1.78 mmol) in tetrahydrofuran (10 mL) was added 4-cyanobenzaldehyde (0.4 g, 2.67 mmol) followed by sodium borohydride and the reaction was heated to 50° C. for 2 hours. On cooling, the reaction was quenched by the addition of water (10 mL) and the aqueous solution basified by the addition of ammonium chloride (˜pH 8). The aqueous mixture was extracted using dichloromethane (3×10 ml) and the organic extracts combined, dried over magnesium sulfate and concentrated in vacuo to afford the title compound as an off white solid (604 mg, 98% yield). HPLC retention time 7.17 min. Mass spectrum (ES+) m/z 397 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08258138B2 |
|---|
| Source dataset | uspto-grants-2012_09 |
|---|
| ORD ID | ord-9606026e63184e11923a209257b8e1db |
|---|
| Source note | uspto-grants-2012_09 |
|---|