HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266528Generated: October 25, 2026
Isopropyl iodide → Methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate
https://huagongshe.com/reaction/266528
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium Sulfide | HCID 14804 | — |
| Reactant | Methyl 3-amino-2-methyl-6-thiocyanatobenzoate | HCID 14801188 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)-benzoate | HCID 54177219 | 75.3% |
Reaction Steps
A suspension of methyl 3-amino-2-methyl-6-thiocyanatobenzoate (22.2 g) in ethanol was added to a solution of sodium sulphide (26.6 g) in water. The resultant mixture was stirred at room temperature for 1 hour and then cooled to 5° C. 2-Iodopropane (19.36 g) was added and the mixture was allowed to warm to room temperature and stirred for 2 hours. It was evaporated to dryness and the residue was suspended in aqueous sodium chloride solution and extracted with dichloromethane. The organic layer was dried (MgSO4) and filtered. The filtrate was evaporated to dryness to give methyl 3-amino-2-methyl-6-(1-methylethylsulphenyl)benzoate (18 g) as a yellow oil NMR(CDCl3) 1.2(d,6H) 2.0(s,3H) 3.0(m, 1H) 3.8(bs,2H) 3.9(s, 1H) 6.5(d, 1H) 7.0(d, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650533 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-351fc97011b0471bb2bcb5843ff1e216 |
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| Source note | uspto-grants-1997_07 |
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