HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256909Generated: October 26, 2026
Potassium Iodide → Methyl 3-iodo-2-methyl-6-(1-methylethylsulphenyl)benzoate
https://huagongshe.com/reaction/2256909
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | Methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate | HCID 54177219 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-iodo-2-methyl-6-(1-methylethylsulphenyl)benzoate | HCID 53891999 | 77.8% |
Reaction Steps
A solution of sodium nitrite (6.7 g) in water was added to a stirred, cooled mixture of methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate (18 g) in concentrated hydrochloric acid while maintaining the temperature below 0° C. The resultant mixture was added to a solution of potassium iodide (16 g) in water while maintaining the temperature at about 80° C. The resultant mixture was stirred at 80° C. for 15 mins then cooled to room temperature. It was diluted with water and extracted with dichloromethane. The organic layer was washed with sodium bicarbonate solution, water, dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give methyl 3-iodo-2-methyl-6-(1-methylethylsulphenyl)benzoate (20.5 g) as a red oil. NMR (CDCl3) 1.25 (d,6H) 2.35(s,3H) 3.2(m, 1H) 3.9(s,3H) 6.9(d, 1H) 7.6(d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05656573 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-12e10774a21f48e9ac5e2890c8b4f7d8 |
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| Source note | uspto-grants-1997_08 |
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