HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 34627Generated: October 30, 2026
Potassium Iodide → HCID 14233447, compound
https://huagongshe.com/reaction/34627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl 2-amino-5-thiocyanatobenzoate | HCID 799394 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14233447 | HCID 14233447 | 32% |
Reaction Steps
To a 500 ml flask fitted with a magnetic stirrer, dropping funnel and thermometer, and containing a solution of 12.7 g (0.192 mol) of 85% potassium hydroxide in 300 ml of methanol was added in portions 10.0 g (0.0481 mol) of methyl 2-amino-5-thiocyanatobenzoate. The solution was cooled to 10° C. and a solution of 6.29 g (0.058 mol) ethylbromide in 50 ml of methanol was added over 10 minutes. This was followed by the addition of 8.0 g (0.048 mol) potassium iodide. After 2.5 hours, the reaction mixture was evaporated to a semi-solid under reduced pressure and treated with 300 ml of water. The aqueous solution was extracted with chloroform, and the organic layer dried over magnesium sulfate. The solution was filtered and evaporated to give 7.5 g (79%) of crude product. This material was recrystallized from hexane to give 3.01 g (32%) of the title compound, m.p. 97°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04762838 |
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| Source dataset | uspto-grants-1988_08 |
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| ORD ID | ord-0319f8da7bf8410aae39305aa0ab16b1 |
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| Source note | uspto-grants-1988_08 |
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