HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307659Generated: November 1, 2026
3-Hydroxybenzaldehyde → HCID 15186783, compound
https://huagongshe.com/reaction/2307659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | p-Fluoronitrobenzene | HCID 9590 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15186783 | HCID 15186783 | 86.6% |
Reaction Steps
3-Hydroxybenzaldehyde (1.15 g, 9.4 mmol), 1-fluoro-4-nitrobenzene (1.0 mL, 9.4 mmol) and K2CO3 (2.61 g, 19 mmol) were combined in DMF (20 mL) and heated at 80° C. After 6 hours, the reaction mixture was cooled to room temperature and partitioned between water and diethyl ether. The separated aqueous phase was extracted with diethyl ether. The organic layers were combined, washed with 1N NaOH, brine, dried (MgSO4), filtered and the filtrate concentrated under reduced pressure to provide the title compound as a yellow solid (1.98 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06831193B2 |
|---|
| Source dataset | uspto-grants-2004_12 |
|---|
| ORD ID | ord-68e1d0d0ece44fcb9c2a6e287e360d78 |
|---|
| Source note | uspto-grants-2004_12 |
|---|