Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2,6-Diiodo-4-nitrophenol | HCID 9370 | — |
| Reactant | Sodium Dithionite | HCID 24489 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-Amino-2-iodophenol | HCID 13774763 | 17.8% |
Reaction Steps
To a yellow suspension of 2,6-diiodo-4-nitrophenol (2.5 g, 6.44 mmol) in 50 mL of 25% NaOH, was added sodium dithionite (36 g) and the reaction mixture was heated and stirred at 75° C., until it was tuned white. After the reaction mixture was cooled to room temperature, 50 mL deionized water was added, and extracted with ethyl acetate (50 mL×5). The combined extracts were washed with water (30 mL×3), brine (30 mL) and dried with Na2SO4. Removed the solvent to give a brown oil, which was purified by flushing chromatography column, eluant with system A Hexane/ethyl acetate (6/1), then system B Hexane/ethyl acetate (3/1) to give a brown solid (0.27 g). 1H-NMR(300 MHz, DMSO): δ9.23 (s, 1H), 7.00˜6.99 (d, 1H), 6.64˜6.61 (d, 1H), 6.52˜6.48 (d, 1H), 5.25 (bs, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08460635B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-f8838971a7cc492591f19edf44fcaff7 |
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| Source note | uspto-grants-2013_06 |
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