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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416442Generated: November 2, 2026

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

https://huagongshe.com/reaction/2416442

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., methanol (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 numberUS06825170B2
Source datasetuspto-grants-2004_11
ORD IDord-4c47923aa4fe4abdbd4f1601d5aec77c
Source noteuspto-grants-2004_11