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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906999Generated: October 26, 2026

18-Crown-6 → 2-Nitro-2-methyl-1-[di-(t-butyl)methoxy]propane

https://huagongshe.com/reaction/1906999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant18-Crown-6HCID 28557—
Reactant2-Nitro-1-propeneHCID 78486—
Reactant2,2,4,4-Tetramethylpentan-3-olHCID 139790—
ReactantCID 53628100HCID 178418400—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
Product2-Nitro-2-methyl-1-[di-(t-butyl)methoxy]propaneHCID 20201202—

Reaction Steps

Di-t-butylmethanol is added to a dry flask under argon at 0° C. Dry tetrahydrofuran is added with a syringe. Sec-Butyl lithium (1.5M in Hexanes) is added quickly in one portion and the contents of the flask are stirred for one hour at room temperature. A 10 mM solution of 18-crown-6-ether in acetonitrile is added with a syringe and the flask cooled to 0° C. A tetrahydrofuran solution of 2-nitropropene is added with vigorous stirring over a 10 minute period. After completion of the reaction, as judged by thin layer chromatography, it is quenched with dimethyl sulfate, poured into saturated ammonium chloride and extracted with ethyl acetate. The organic layer is dried over MgSO4 and evaporated to yield 2-nitro-2-methyl-1-[di-(t-butyl)methoxy]propane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04654439
Source datasetuspto-grants-1987_03
ORD IDord-a721fd9b46e9420e949ffa01b97e77ca
Source noteuspto-grants-1987_03