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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095702Generated: October 30, 2026

Methyl iodide → 1-((S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-4-iodo-5-methyl-1H-pyrazole

https://huagongshe.com/reaction/2095702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantCyclohexaneHCID 8078—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium diisopropylamideHCID 2724682—
Reactant1-{[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methyl}-4-iodo-1H-pyrazoleHCID 67004425—
Product1-((S)-2,2-dimethyl-[1,3]dioxolan-4-ylmethyl)-4-iodo-5-methyl-1H-pyrazoleHCID 67004621—

Reaction Steps

A solution of 1-{[(4S)-2,2-Dimethyl-1,3-dioxolan-4-yl]methyl}-4-iodo-1H-pyrazole (700 mg, 2.27 mmol) in THF (6 mL, 70 mmol) was cooled to −78° C., and 1.5 M of LDA in cyclohexane (4.5 mL, 6.8 mmol) was added. After stirring for 1 h, methyliodide (1.41 mL, 22.7 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 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445510B2
Source datasetuspto-grants-2013_05
ORD IDord-bb40d9fec41c4e78a65e59a3bc46e9f1
Source noteuspto-grants-2013_05