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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692920Generated: November 1, 2026

Chloromethyl Methyl Ether → 1-(Methoxymethyl)-3-methylidenecyclobutane-1-carbonitrile

https://huagongshe.com/reaction/1692920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
Reactant3-MethylenecyclobutanecarbonitrileHCID 27474—
ReactantLithium diisopropylamideHCID 2724682—
SolventTetrahydrofuranHCID 8028—
Product1-(Methoxymethyl)-3-methylidenecyclobutane-1-carbonitrileHCID 66824307—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of 3-methylenecyclobutanecarbonitrile (1.00 g, 0.0107 mol) in tetrahydrofuran (40 mL, 0.5 mol) was added 2.00 M of lithium diisopropylamide in tetrahydrofuran (6.44 mL) at −78° C. After stirred at −78° C. for 30 min, to the resulting mixture was added chloromethyl methyl ether (1.02 mL, 0.0134 mol). The reaction was stirred at −78° C. for 30 min, then allowed to warm up to rt, quenched with ammonium chloride, then extracted with ether. The combined organic layers were washed with water, brine, dried, and evaporated to dryness. The crude residue was used directly in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158616B2
Source datasetuspto-grants-2012_04
ORD IDord-6e3d1f578ef742da9d5304a0b7f70c9c
Source noteuspto-grants-2012_04