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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 380317Generated: November 2, 2026

Ammonia → 4-(Bicyclo[2.2.1]hept-1-yl)-3,6-dichloropyridazine

https://huagongshe.com/reaction/380317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSulfuric AcidHCID 1118—
ReactantAmmonium PersulfateHCID 62648—
Reactant3,6-DichloropyridazineHCID 67331—
ReactantBicyclo(2.2.1)heptane-1-carboxylic acidHCID 140414—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
Product4-(Bicyclo[2.2.1]hept-1-yl)-3,6-dichloropyridazineHCID 1836494698.7%

Reaction Conditions

Temperature70 °C

Reaction Steps

Concentrated sulphuric acid (2.17 ml, 40 mM) was added carefully to a suspension of 3,6-dichloropyridazine (2.11 g, 14.3 mM) in water (50 ml). This mixture was then heated to 70° C. and bicyclo[2.2.1]heptane-1-carboxylic acid (Org. Synth., 59, 85; 2.0 g, 14.3 mM) was added. After ten minutes a solution of silver nitrate (0.48 g, 2.8 mM) in water (5 ml) was added dropwise over two minutes. A solution of ammonium persulphate (9.8 g, 43 mM) in water (20 ml) was added over 20 minutes. The reaction was heated at 70° C. for a further 40 minutes and then allowed to cool to room temperature. The mixture was poured onto ice and basified with concentrated aqueous ammonia; the temperature was kept below 10° C. by addition of more ice. The aqueous phase was extracted with dichloromethane (3×200 ml) and the combined extracts were dried (MgSO4), filtered and evaporated to give the crude product, which was purified by column chromatography using ethyl acetate/hexane mixtures as the eluent to give the title compound (3.4 g). 1H NMR (250 MHz, CDCl3) δ1.49-2.00 (8H, m), 2.17 (2H, m), 2.43 (1H, m), 7.45 (1H, s); MS (ES+) m/e 244 [MH]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06303597B1
Source datasetuspto-grants-2001_10
ORD IDord-f136de486a904972a2deea84bad56575
Source noteuspto-grants-2001_10