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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604611Generated: October 31, 2026

Isoamyl Nitrite → 6-Iodoindane-5-carbonitrile

https://huagongshe.com/reaction/604611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantIodide IonHCID 30165—
Reactant6-amino-2,3-dihydro-1H-indene-5-carbonitrileHCID 45122176—
SolventChloroformHCID 6212—
Product6-Iodoindane-5-carbonitrileHCID 57576269—

Reaction Steps

A mixture of 6-aminoindane-5-carbonitrile (48.5 mg, 0.307 mmol), isoamyl nitrite (82 μL, 0.614 mmol) and iodide (85.7 mg, 0.338 mmol) in dry CHCl3 (2 mL) was stirred at room temperature for 0.5 h. The mixture was then heated at 80° C. under N2 for 2 h. The reaction mixture was quenched with saturated Na2S2O3 and partitioned between CH2Cl2 and water. The organic layer was dried (Na2SO4) and concentrated in vacuo. The residue was purified by flash chromatography (Si, 1% EtOAc in hexanes) to afford 6-iodoindane-5-carbonitrile. LCMS calc.=270.0; found=270.0 (M+1)+. 1H NMR (500 MHz, CDCl3) δ 7.78 (s, 1H), 7.48 (s, 1H), 2.96 (t, J=7.5 Hz, 2H), 2.92 (t, J=7.5 Hz, 2H), 2.16-2.10 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07910592B2
Source datasetuspto-grants-2011_03
ORD IDord-db9018ef49c042158934b1e46d0db72c
Source noteuspto-grants-2011_03