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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452388Generated: October 26, 2026

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

https://huagongshe.com/reaction/452388

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 numberUS08492373B2
Source datasetuspto-grants-2013_07
ORD IDord-4babd4090a13468b9b4767832da2b11a
Source noteuspto-grants-2013_07