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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494197Generated: October 30, 2026

Iodine → 5-Iodo-7-nitro-1-trifluoroacetyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/494197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
Reactant7-Nitro-1-trifluoroacetyl-1,2,3,4-tetrahydroquinolineHCID 12578361—
ReactantPotassium IodateHCID 23665710—
SolventSulfuric AcidHCID 1118—
Product5-Iodo-7-nitro-1-trifluoroacetyl-1,2,3,4-tetrahydroquinolineHCID 8585634036.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 7-nitro-1-trifluoroacteyl-1,2,3,4-tetrahydroquinoline (D4) (2 g, 7.3 mmol) in conc. sulfuric acid (10 ml) was cooled to 0° C. and treated with iodine (1.11 μg, 4.4 mmol) and potassium iodate (0.625 g, 2.9 mmol). The reaction was stirred at 0° C. for 3 h then room temperature for 2 h. The reaction mixture was slowly poured into water (150 ml) at 0° C. and extracted with DCM. This was washed with aq. sodium metabisulfite and water then dried over MgSO4 and concentrated in vacuo to give the crude product. Purification by column chromatography gave the title compound (420 mg). 1H NMR (250 MHz, CDCl3) δ (ppm): 8.59 (m, 2H), 3.86 (m, 2H), 2.90 (t, 2H), 2.17 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538121B2
Source datasetuspto-grants-2009_05
ORD IDord-07b3bb6d5e234fd5981cc4fe45ab812e
Source noteuspto-grants-2009_05