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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714735Generated: October 30, 2026

8-Nitroquinoline → 3-Iodo-8-nitroquinoline

https://huagongshe.com/reaction/1714735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-NitroquinolineHCID 11830—
ReactantN-IodosuccinimideHCID 120273—
SolventAcetic AcidHCID 176—
Product3-Iodo-8-nitroquinolineHCID 1203236798.2%

Reaction Conditions

Temperature62 °C

Reaction Steps

A stirred mixture of 8-nitroquinoline (100 g, 0.57 mol) in acetic acid (500 ml) was treated with N-iodosuccinimide (155 g, 0.69 mol) portionwise over 10 minutes, and warmed to 62° C. for 6 h. A further portion of N-iodosuccinimide (25 g, 0.14 mol) was introduced and the mixture stirred for a further 16 h before cooling to ambient temperature. The solvent was removed in vacuo, keeping the temperature below 35° C. The residue was dissolved in dichloromethane (2 L) and washed successively with saturated aqueous sodium bicarbonate solution (2×1 L), 10% aqueous sodium thiosulphate solution (1 L), water (1 L), brine (100 ml), then the organic phase was dried over magnesium sulphate. The mixture was filtered and the solvent removed to give a yellow solid which was recrystallised from ethyl acetate to give the title compound (D3) (168 g, 97%) as a yellow solid;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799774B2
Source datasetuspto-grants-2010_09
ORD IDord-1efc24cc7936423286248d3e44073169
Source noteuspto-grants-2010_09