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n-Butyl chloride. Identifiers ... It can be prepared from 1-butanol by treatment with hydrogen chloride. [4] It reacts with lithium metal to give n-butyllithium: [5]
In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane. The isomer n -butane can connect in two ways, giving rise to two "-butyl" groups:
Butyl chloride (C 4 H 9 Cl) may refer to: n-Butyl chloride (butan-1-chloride) sec-Butyl chloride (butan-2-chloride) Isobutyl chloride (1-chloro-2-methylpropane)
Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with sodium amalgam. [4] Neopentyl alcohol can be converted to neopentyl iodide by treatment with triphenylphosphite/methyl iodide: [5]
tert-Butyl chloride is the organochloride with the formula (CH 3) 3 CCl. It is a colorless, flammable liquid. It is sparingly soluble in water, with a tendency to undergo hydrolysis to the corresponding tert-butyl alcohol. It is produced industrially as a precursor to other organic compounds. [1]
Neophyl chloride, C 6 H 5 C(CH 3) 2 CH 2 Cl, is a halogenated organic compound with unusual nucleophilic substitution properties. Neophyl chloride is used to form a versatile organolithium reagent , neophyl lithium, by reaction with lithium.
n-Butylamine is an organic compound (specifically, an amine) with the formula CH 3 (CH 2) 3 NH 2.This colourless liquid is one of the four isomeric amines of butane, the others being sec-butylamine, tert-butylamine, and isobutylamine.
Pentanenitrile, valeronitrile or butyl cyanide is a nitrile with the formula C 4 H 9 CN. This can be written BuCN, with Bu representing an n-butyl (linear butyl group).