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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiiodomethaneHCID 6346—
Reactant5-(Methoxymethoxy)-2-(2-methylprop-1-enyl)pyridineHCID 67270997—
ReactantHCID 178418750HCID 178418750—
SolventTolueneHCID 1140—
Product2-(2,2-Dimethylcyclopropyl)-5-(methoxymethoxy)pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552181B2
Source datasetuspto-grants-2013_10
ORD IDord-8ecaf7ba2dd240caafc2c88786fe6aa6
Source noteuspto-grants-2013_10