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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307659Generated: November 1, 2026

3-Hydroxybenzaldehyde → HCID 15186783, compound

https://huagongshe.com/reaction/2307659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
ProductHCID 15186783HCID 1518678386.6%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831193B2
Source datasetuspto-grants-2004_12
ORD IDord-68e1d0d0ece44fcb9c2a6e287e360d78
Source noteuspto-grants-2004_12