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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972748Generated: November 1, 2026

Hydrazine, (phenylmethyl)-, hydrochloride (1:1) → HCID 58529737, compound

https://huagongshe.com/reaction/1972748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine, (phenylmethyl)-, hydrochloride (1:1)HCID 14084—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
Solvent1-ButanolHCID 263—
ProductHCID 58529737HCID 5852973750%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a dried flask charged with 4-bromo-2-fluorobenzonitrile (5.0 g, 22.5 mmol) in n-butanol (60 mL) was added a solution of benzylhydrazine hydrochloride (17.56 g, 90 mmol, 4.0 eq) and diisopropylethylamine (32.1 mL, 184.48 mmol, 8.2 eq). The reaction mixture was stirred at 140° C. under N2 for 3 days. The mixture was cooled to rt and partitioned between EtOAc and water. The organic layer was washed with saturated aqueous NaHCO3, water, brine, dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified using an ISCO® instrument (gradient 5 to 60% EtOH/DCM) and the product containing fractions were concentrated to give 3.4 g (50%) of the title compound as beige solid. 1H NMR (300 MHz, CD2Cl2) δ 7.63 (dd, 1H), 7.37 to 7.30 (m, 4H), 7.20 to 7.16 (m, 2H), 6.94 (dd, 1H), 5.44 (s, 2H), 4.02 (broad s, 2H); ES-MS m/z 302.3/304.3 [M+H]+, RT (min) 2.34.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431695B2
Source datasetuspto-grants-2013_04
ORD IDord-10a9439fc95c46ccb29551cfaf151dc7
Source noteuspto-grants-2013_04