HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447235Generated: October 29, 2026
Hydrochloric Acid → 4-Iodo-2,6-dimethylaniline hydrochloride
https://huagongshe.com/reaction/447235
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,6-Dimethylaniline | HCID 6896 | — |
| Reactant | Iodine chloride | HCID 24640 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Iodo-2,6-dimethylaniline hydrochloride | HCID 57348210 | — |
Reaction Steps
To a suspension of sodium bicarbonate (126 g, 1.5 moles) and 2,6-dimethylaniline (61.5 mL, 500 mmoles) in methanol (700 mL) was added iodine monochloride (1.0 M in dichloromethane, 550 mL, 550 mmoles) at room temperature over 1 h. After addition was complete, stirring was continued for 3 h. The reaction was filtered to remove excess sodium bicarbonate and the solvent removed in vacuo. The residue was re-dissolved in diethyl ether (1.5 L) and treated with hydrochloric acid (2M in ether, 375 mL, 750 mmoles). The resulting suspension was stored in the freezer (−15° C.) overnight. The solid was filtered and washed with diethyl ether until it became colorless, to give 126.5 g (89%) as a grey-green powder. 1H-NMR (DMSO-d6) δ 2.33 (s, 6H), 7.48 (s, 2H), 9.05 (bs, 3H); 13C-NMR (DMSO-d6) δ 17.4, 91.5, 133.1, 131.2, 136.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481546B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9d8440480efa4499af1eec4c3b933fbc |
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| Source note | uspto-grants-2013_07 |
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