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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Nitro-1-trifluoroacetyl-1,2,3,4-tetrahydroquinoline | HCID 12578361 | — |
| Reactant | Potassium Iodate | HCID 23665710 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 5-Iodo-7-nitro-1-trifluoroacetyl-1,2,3,4-tetrahydroquinoline | HCID 85856340 | 36.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538121B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-07b3bb6d5e234fd5981cc4fe45ab812e |
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| Source note | uspto-grants-2009_05 |
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