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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906120Generated: October 26, 2026

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

https://huagongshe.com/reaction/1906120

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 1-[di-(t-butyl)methoxy]propaneHCID 13907245—

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 saturated ammonium chloride and extracted with ethyl acetate. The organic layer is dried over MgSO4 and evaporated to yield 2-nitro 1-[di-(t-butyl)methoxy]propane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04650688
Source datasetuspto-grants-1987_03
ORD IDord-9c239f608e2445dab4bc3d523d57bfc9
Source noteuspto-grants-1987_03