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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710412Generated: November 2, 2026

3-Fluorobenzonitrile → HCID 178513300, compound

https://huagongshe.com/reaction/1710412

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-FluorobenzonitrileHCID 67880—
ReactantDiisopropylethylamineHCID 81531—
ReactantHydroxyamine hydrochlorideHCID 443297—
SolventEthanolHCID 702—
ProductHCID 178513300HCID 17851330089%

Reaction Conditions

Temperature70 °C

Reaction Steps

3-Fluorobenzonitrile (2.5 g, 0.021 mol), diisopropylethyl amine (10.8 mL, 0.062 mol) and hydroxylamine hydrochloride (4.3 g, 0.062 mol) were mixed in ethanol (30 mL). The reaction mixture was stirred at 70° C. overnight. The reaction mixture was cooled to room temperature and concentrated to half the original volume. The residue was added to a mixture of dichloromethane (200 mL) and water (60 mL). The mixture was basified to pH 9 using 2N NaOH and the organic phase was separated. The aqueous phase was extracted further with dichloromethane (2×50 mL) and the combined organic phase was washed with water (75 mL), washed with brine (75 mL), dried over sodium sulfate and concentrated to give the product as a yellow solid (2.8 g, 89%). 1H NMR (300 MHz, CDCl3): δ 8.05 (bs, 1H), 7.39 (m, 3H), 7.16 (m, 1H), 4.88 (bs, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790717B2
Source datasetuspto-grants-2010_09
ORD IDord-3cad777ffd6c457282227115756393fd
Source noteuspto-grants-2010_09