HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804506Generated: November 2, 2026
N-Iodosuccinimide → Methyl 4-iodo-5-isobutylisoxazole-3-carboxylate
https://huagongshe.com/reaction/1804506
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | Methyl 5-isobutylisoxazole-3-carboxylate | HCID 3477558 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | Methyl 4-iodo-5-isobutylisoxazole-3-carboxylate | HCID 58374143 | 78% |
Reaction Steps
A mixture of methyl 5-isobutylisoxazole-3-carboxylate (0.923 g, 5.04 mmol) and N-iodosuccinimide (1.25 g, 5.54 mmol) in trifluoroacetic acid (25 mL) was stirred at room temperature overnight. By HPLC, the reaction was complete. The trifluoroacetic acid was removed under reduced pressure, and the residue was diluted with dichloromethane (100 mL), washed with a saturated aqueous solution of sodium bicarbonate (2×25 mL), washed with a 2.5% aqueous solution of sodium bisulfate (25 mL), and dried over anhydrous sodium sulfate. Concentration under reduced pressure followed by purification by flash silica gel chromatography using a 5% mixture of ethyl acetate in hexane afforded methyl 4-iodo-5-isobutylisoxazole-3-carboxylate (1.21 g, 3.91 mmol, 78% yield) as a pale yellow oil. The product had an HPLC ret. time=2.40 min.−Column: CHROMOLITH® SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=310.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354398B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-978a07962a504cfbb6565f4ab3a738cd |
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| Source note | uspto-grants-2013_01 |
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