HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487966Generated: October 31, 2026
Iodine → Methyl 4-cyclopropyl-5-iodo-2-methylbenzoate
https://huagongshe.com/reaction/1487966
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl 4-cyclopropyl-2-methylbenzoate | HCID 59020660 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Methyl 4-cyclopropyl-5-iodo-2-methylbenzoate | HCID 68288233 | 47.2% |
Reaction Steps
To a solution of methyl 4-cyclopropyl-2-methylbenzoate (compound 86.1, 2.68 g, 13.4 mmol, 95%) in AcOH (50 mL) were added NaIO4 (1.51 g, 7.08 mmol), iodine (3.58 g, 14.1 mmol), and sulfuric acid (106 μL, 2.0 mmol, 0.15 equiv). The reaction mixture was stirred overnight at 110° C. After cooling to ambient temperature, water (100 mL) was slowly added and the mixture was extracted with ethyl acetate (100 mL). The organic layer was washed with Na2S2O3 (aq., sat., 3×30 mL) and brine (30 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1/50) as the eluent to yield 2.0 g (45%) of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-96bb2dff44c64183bf130e648124a312 |
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| Source note | uspto-grants-2016_08 |
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