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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271131Generated: November 1, 2026

8-Nitroquinoline → 3-Iodo-8-nitroquinoline

https://huagongshe.com/reaction/271131

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 numberUS07452888B2
Source datasetuspto-grants-2008_11
ORD IDord-ba7bfc0b5290448994137ca1a072f1b7
Source noteuspto-grants-2008_11