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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1064820Generated: November 1, 2026

Triethylamine → HCID 22272835, compound

https://huagongshe.com/reaction/1064820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDiisopropylanilineHCID 32484—
Reactant4-Bromobutanoyl bromideHCID 13542246—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 22272835HCID 2227283563.1%

Reaction Steps

To a solution of 2,6-diisopropylaniline (1.77 g, 10 mmol) in chloroform (30 ml) was added triethylamine (1.11 g, 11 mmole), then 4-bromobutyryl bromide (1.95 mg, 10.5 mmol) was slowly dropped thereinto with ice cooling and the mixture was made to react for 20 minutes. The reaction solution was diluted with water and extracted with chloroform. The organic layer was washed with 0.5N HCl, water, aqueous solution of sodium bicarbonate and saturated sodium chloride solution successively and dried over magnesium sulfate and the solvent was evaporated therefrom. The residue was purified by a silica gel column chromatography (120 g of silica gel; developing solvent, hexane:acetone=7:1→5:1) and the resulting crude crystals were recrystallized from hexane-acetone to provide 2.06 g (yield 63%) of 4-bromo-N-(2,6-diisopropylphenyl)butyramide as colorless needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06969711B2
Source datasetuspto-grants-2005_11
ORD IDord-0a4e545abb644d51bb2d5f945484b759
Source noteuspto-grants-2005_11