HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039724Generated: October 30, 2026
Diiodomethane → 2-(2,2-Dimethylcyclopropyl)-5-(methoxymethoxy)pyridine
https://huagongshe.com/reaction/1039724
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diiodomethane | HCID 6346 | — |
| Reactant | 5-(Methoxymethoxy)-2-(2-methylprop-1-enyl)pyridine | HCID 67270997 | — |
| Reactant | HCID 178418750 | HCID 178418750 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2,2-Dimethylcyclopropyl)-5-(methoxymethoxy)pyridine | HCID 57950926 | — |
Reaction Steps
Diiodomethane (24.8 ml, 308 mmol) was added dropwise to a solution of diethylzinc (200 ml, 220 mmol) 1.1 M in toluene at 0° C. After the addition, the solution was stirred at RT for 40 minutes and then recooled to 0° C. when 5-(methoxymethoxy)-2-(2-methylprop-1-enyl)pyridine (21.3 g, 110 mmol) in toluene (150 mL) was added dropwise through an addition funnel. The reaction was allowed to come to RT and was stirred 12 hrs before being quenched at 0° C. by the addition of a 10:1 saturated ammonium chloride/ammonium hydroxide aqueous solution. The layers were separated and the aqueous layer was diluted with water and extracted into ethyl acetate. The combined organic layers were washed with 10:1 saturated ammonium chloride/ammonium hydroxide aqueous solution, water, brine, dried over sodium sulfate, and concentrated. The crude product was purified through a plug of silica (10:1 Hexanes/EtOAc) to afford the titled compound. MS m/z: 208.2 (100%, M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552181B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-8ecaf7ba2dd240caafc2c88786fe6aa6 |
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| Source note | uspto-grants-2013_10 |
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