Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2,6-Dichloroaniline | HCID 11846 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2,6-Dichloro-4-iodobenzenamine | HCID 12770 | — |
Reaction Steps
2,6-Dichloroaniline (16.2 g, 0.1 mol) is suspended in a solution of sodium bicarbonate (8.6 g, 0.1 mol in 100 mL of water) and warmed to 60° C. Elemental iodine (25.4 g, 0.1 mol) is added portionwise and the resulting mixture stirred at 60° C. for 3 days. After cooling to room temperature, the reaction mixture is partitioned between CH2Cl2 (250 mL) and saturated sodium bisulfite solution (500 mL). The aqueous layer is re-extracted with additional CH2Cl2 (250 mL) and the combined organic layers dried (MgSO4) and concentrated by rotary evaporator. The residual oil is purified by flash chromatography (9:1 hexanes/EtOAc) to give 2,6-dichloro-4-iodoaniline (m.p. 100–102° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202364B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-f13304d88833498182617bbccea22fb7 |
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| Source note | uspto-grants-2007_04 |
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