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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722504Generated: October 31, 2026

tert-BUTYL CHLORIDE → 2,2,4,4-Tetramethyl-3-pentanone Imine

https://huagongshe.com/reaction/1722504

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-BUTYL CHLORIDEHCID 10486—
ReactantPivalonitrileHCID 12416—
ReactantSodiumHCID 5360545—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChlorobenzeneHCID 7964—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product2,2,4,4-Tetramethyl-3-pentanone ImineHCID 2755632—

Reaction Steps

This was prepared by the method of J. Chem. Soc., Perkin I, 2087 (1976); ibid, 1797 (1974). Pivalonitrile (33.2 g.) and t-butyl chloride (44.4 g.) were added under nitrogen to a well stirred suspension of sodium sand (18.4 g.) in a mixture of hexane (80 ml.), tetrahydrofuran (20 ml.) and methanol (1 ml.) over one hour at 15°-20° C. The mixture was stirred three hours, a solution of chlorobenzene (2 g.) in tetrahydrofuran (5 ml.) added dropwise over 10 minutes and stirring continued for one hour. Methanol (20 ml.) was added with caution over 0.5 hr. followed by water until phases separated. The aqueous phase was extracted with ether and the combined organic phases dried and evaporated in vacuo. The residue was distilled to afford di-t-butylketone imine, b.p. 62°-63° C./19 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855454
Source datasetuspto-grants-1989_08
ORD IDord-18e0ac6bf12549f09a3a3d59acba9992
Source noteuspto-grants-1989_08