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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166085Generated: October 29, 2026

Hydrochloric Acid → 2-Fluoro-4-(1H-pyrazol-1-yl)benzaldehyde

https://huagongshe.com/reaction/1166085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantDiisobutylaluminumhydrideHCID 21225700—
Reactant2-Fluoro-4-(1H-pyrazol-1-yl)benzonitrileHCID 22631184—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product2-Fluoro-4-(1H-pyrazol-1-yl)benzaldehydeHCID 2263102665%

Reaction Steps

Diisobutylaluminum hydride (1.0 M in toluene, 11.00 mL, 11.00 mol) was added dropwise over 10 min to a vigorously stirred suspension of the compound from step A (1.88 g, 10.04 mmol) in toluene (100 mL) at −78° C. After 1 h at −78° C., MeOH (1 mL) was added, the mixture was stirred for 5 min, and then poured into a stirred, cold (0° C.) mixture of 1.2 N HCl (100 mL) and ethyl acetate (100 mL). After stirring for 30 min at RT, the layers were separated and the aqueous layer was extracted with additional ethyl acetate (100 mL). The combined organic layers were washed with sat. aq. NaHCO3 (100 mL) and brine (100 mL), dried (MgSO4), and concentrated. Recrystallization from IPA followed by chromatography (SiO2, dichloromethane) provided 1.25 g (65%) of the title compound as a colorless solid. MS 191 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613747B2
Source datasetuspto-grants-2003_09
ORD IDord-3781f59248a140a1852d05f2f9099c27
Source noteuspto-grants-2003_09