HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67650Generated: October 28, 2026
Methyl iodide → HCID 13073255, compound
https://huagongshe.com/reaction/67650
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 4-amino-3-[3-(trifluoromethyl)phenyl]-1,2-thiazole-5-carboxylate | HCID 13073199 | — |
| Reactant | HCID 20265399 | HCID 20265399 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13073255 | HCID 13073255 | — |
Reaction Steps
A suspension of 0.5 g. of sodium hydride (washed free of mineral oil) in 15 ml. of tetrahydrofuran was cooled to -20° C. and stirred. To the cold stirred suspension was added in one portion 3.0 g. of methyl 3-(3-trifluoromethylphenyl)-4-amino-5-isothiazolecarboxylate. The reaction mixture was warmed to room temperature, at which time 1.5 ml. of methyl iodide was added in one portion. The reaction mixture was stirred at ambient temperature for two hours, and then was added to 50 ml. of ice water. The aqueous mixture was extracted several times with diethyl ether. The ethereal extracts were combined, washed with water, dried and the solvent was removed by evaporation under reduced pressure to afford 2.0 g. of methyl 4-methylamino-3-(3-trifluoromethylphenyl)-5-isothiazolecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04346094 |
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| Source dataset | uspto-grants-1982_08 |
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| ORD ID | ord-c0df6d52a0734ee18176b4e4379b42e5 |
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| Source note | uspto-grants-1982_08 |
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