HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 270739Generated: October 29, 2026
Hydrochloric Acid → 4-Iodo-2,6-dimethylaniline hydrochloride
https://huagongshe.com/reaction/270739
Participants
| Role | Name | HCID | Charge |
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| 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, 1500 mmol) and 2,6-dimethylaniline (61.5 mL, 500 mmol) in methanol (700 mL) was added iodine monochloride (1.0 M in dichloromethane, 550 mL, 550 mmol) 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 redissolved in diethyl ether (1.5 L) and treated with hydrochloric acid (2M in ether, 375 mL, 750 mmol). 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 | US07449586B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-d454fe3234c8403a9e6b8eeeb6cedcd9 |
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| Source note | uspto-grants-2008_11 |
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