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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359859Generated: October 26, 2026

Iodoethane → HCID 20063997, compound

https://huagongshe.com/reaction/359859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
ReactantLithium diisopropylamideHCID 2724682—
Reactant5-(5-Bromopentyl)-3-methylisoxazoleHCID 13544046—
Reactant3,5-Dichloro-4-methylbenzoic acidHCID 18533234—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventHexamethylphosphoramideHCID 12679—
ProductHCID 20063997HCID 20063997—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 1.2 ml hexamethylphosphoramide and 6.7 ml 1.75M lithium diisopropylamide in 9 ml tetrahydrofuran at 0° C. under nitrogen was slowly added a solution of 1.00 g 3,5-dichloro-4-methylbenzoic acid in 3 ml tetrahydrofuran. After 1 hr the solution was cooled to -78° C. and 1.00 g 5-(5-bromopentyl)-3-methylisoxazole was added. The reaction mixture was stirred at room temperature for 19 hrs and worked up by acid-base extraction to give 1.3 g crude acid product. The latter was treated with 1 ml ethyl iodide and 4.9 g potassium carbonate in 10 ml dimethylformamide, stirred 12 hrs at room temperature. Extraction with ether and washing with water provided 1 g of ethyl 3,5-dichloro-4-[6-(3-methyl-5-isoxazolyl)hexyl]benzoate suitable for subsequent reactions.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05002960
Source datasetuspto-grants-1991_03
ORD IDord-3c081daa015c43acaf04c9a1c97bbaca
Source noteuspto-grants-1991_03