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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966146Generated: October 31, 2026

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

https://huagongshe.com/reaction/1966146

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 numberUS08420629B2
Source datasetuspto-grants-2013_04
ORD IDord-5e391a27177e4a698d203b9e2ff53cd5
Source noteuspto-grants-2013_04