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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406136Generated: October 26, 2026

Hydrazine → 2-Hydrazinyl-5,6,7,8,9,10-hexahydrocyclooct[b]pyridine

https://huagongshe.com/reaction/2406136

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant2-Chloro-5,6,7,8,9,10-hexahydrocycloocta[b]pyridineHCID 58199532—
SolventEthanolHCID 702—
Product2-Hydrazinyl-5,6,7,8,9,10-hexahydrocyclooct[b]pyridineHCID 55281928—

Reaction Conditions

Temperature150 °C

Reaction Steps

2-Chloro-5,6,7,8,9,10-hexahydrocycloocta[b]pyridine was treated with ethanol (20 mL) and anhydrous hydrazine (5 mL) in a sealed tube at 150° C. bath temperature for 7 h. Initial experiments showed that the addition did not proceed in boiling ethanol at atmospheric pressure. HPLC showed that the addition was incomplete, so the reaction mixture was heated at 150° C. for a further 7 h. The solvent was removed under reduced pressure and the residue was purified by flash chromatography on silica gel, eluting with 95% dichloromethane and 5% of a 2M solution of ammonia in methanol; 1H NMR (CDCl3, 300 MHz) 7.19 (d, 1H), 6.51 (d, 1H), 5.85 (br s, 1H), 3.77 (br s, 2H), 2.79 (m, 2H), 2.63 (m, 2H), 1.73 (m, 2H), 1.62 (m, 2H), 1.36 (m, 4H) ppm; 13C NMR (CDCl3, 75 MHz) 156.87, 158.54, 138.81, 126.67, 104.58, 34.72, 32.67, 31.45, 30.85, 26.41, 26.37; MS (ES) 192 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809347B2
Source datasetuspto-grants-2014_08
ORD IDord-7c395deb5c66452e8bf3ccdcf8d1a12d
Source noteuspto-grants-2014_08