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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1484517Generated: October 30, 2026

Cyclopropanecarbonitrile → 1-[2,6-Bis(methoxymethoxy)-3-methyl-phenyl]cyclopropanecarbonitrile

https://huagongshe.com/reaction/1484517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarbonitrileHCID 79637—
Reactant2-Fluoro-1,3-bis(methoxymethoxy)-4-methyl-benzeneHCID 72704334—
ReactantHCID 178504302HCID 178504302—
SolventTolueneHCID 1140—
Product1-[2,6-Bis(methoxymethoxy)-3-methyl-phenyl]cyclopropanecarbonitrileHCID 9001482242.7%

Reaction Conditions

Temperature105 °C

Reaction Steps

2-fluoro-1,3-bis(methoxymethoxy)-4-methyl-benzene (Intermediate 34, 17.5 g, 76.011 mmol) and cyclopropanecarbonitrile (22.625 g, 337.23 mmol) were warmed under stirring to 105° C. A solution of [bis(trimethylsilyl)amino]potassium 0.5M in Toluene (275 ml) was slowly added for 1 hour to the previous solution. The reaction mixture was stirred for 6 hour at the same temperature. After cooling the solid was filtered off and the filtrate was partitioned between Brine (200 ml) and ethyl acetate (300 ml). The aqueous layer was re-extracted with ethyl acetate (200 ml) and combined organic layers were dried (Na2SO4), filtered and evaporated (the temperature during the concentration was ˜60° C. for removing the excess of cyclopropane carbonitrile). The residue was triturated with isopropanol (25 ml) and the solid collected and dried to afford the title compound (9.0 g) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422252B2
Source datasetuspto-grants-2016_08
ORD IDord-d48bf122405f4ceaaae32918cf85162e
Source noteuspto-grants-2016_08