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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 476957Generated: October 30, 2026

1-Iodopropane → HCID 14012385, compound

https://huagongshe.com/reaction/476957

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-IodopropaneHCID 33643—
ReactantN-(3-chloro-2-methylphenyl)-2,2-dimethylpropanamideHCID 4204423—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 14012385HCID 1401238597%

Reaction Steps

A solution of 3-chloro-N-(2,2-dimethylpropionyl)-2-methylaniline (9.79 g) in dry THF (150 ml) was stirred under nitrogen at 0° while a solution of n-butyllithium in hexane was added in a dropwise fashion until a slight orange color was noted. The volume of n-butyllithium solution which had been added was noted, and an equal volume of this n-butyllithium solution was then added in order to complete formation of the dianion of the starting material. The final deep orange solution was then stirred at 0° for 15 min before adding iodopropane (7.92 g). After 15 min, the reaction mixture was cautiously diluted with water (250 ml) and was extracted with ethyl ether (300 ml). The organic layer was washed with brine, dried (MgSO4), and evaporated to afford the title compound as a white solid, 11.38 g (97% yield). Recrystallization from hexane provided an analytical sample, m.p. 88°-89°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886800
Source datasetuspto-grants-1989_12
ORD IDord-728a6cbc474b4af9bf27a17d909bbd1d
Source noteuspto-grants-1989_12