HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095719Generated: November 2, 2026
Methyl iodide → 1-{[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl}-4-iodo-5-methyl-1H-pyrazole
https://huagongshe.com/reaction/2095719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | 1-{[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl]methyl}-4-iodo-1H-pyrazole | HCID 67004091 | — |
| Product | 1-{[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]methyl}-4-iodo-5-methyl-1H-pyrazole | HCID 67004617 | — |
Reaction Steps
To a solution of 1-{[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl]methyl}-4-iodo-1H-pyrazole (500 mg, 1.62 mmol) in THF (4 mL, 50 mmol), cooled to −78° C., was added 1.5 M of LDA in cyclohexane (3.25 mL, 4.87 mmol). After stirring for 1 h, methyliodide (1.01 mL, 16.2 mmol) was added slowly, and the mixture was stirred at −78° C. for 1 h. Sat. NH4Cl was added to quench, and the organic solvent was removed in vacuo. The material was extracted with DCM and water, and the organic layer was concentrated in vacuo. The material was purified via column chromatography, eluting with 5-10% EtOAc/hexanes. The fractions containing the pure product were concentrated in vacuo to afford the title compound as a white solid. MS (ES+): m/z=323.06 (100) [MH+]. HPLC: tR=1.20 min (polar—3 min, UPLC-ACQUITY).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445510B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-562bb94c2aea4c85b814f4bdd4218b21 |
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| Source note | uspto-grants-2013_05 |
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