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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 426621Generated: October 26, 2026

Oxalyl chloride → 2-[6-(Chloroformyl)hexyl]cyclopent-2-en-1-one

https://huagongshe.com/reaction/426621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-Oxo-1-cyclopentene-1-heptanoic acidHCID 78902—
ReactantSodiumHCID 5360545—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2-[6-(Chloroformyl)hexyl]cyclopent-2-en-1-oneHCID 20287596—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 1.94 g (0.08 mol) of sodium hydri in 100 ml of tetrahydrofuran is added with stirring under argo dropwise a solution of 17 g (0.08 mol) of 2-(6-carboxyhexyl)-cyclopent-2-en-1-one in 160 ml of tetrahydrofuran. After the addition is complete, the mixture is stirred for 1 hour 15 minutes. The mixture is cooled to 0° C. and 13 ml of oxalyl chloride is added. The mixture is stirred at 0° C. for 30 minutes and at room temperature for 30 minutes. The solution is diluted with 500 ml of ether and filtered through Celite. The solvent is removed from the filtrate and the residue is extracted with hot hexane twice. The hexane is removed to give 16.0 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04170597
Source datasetuspto-grants-1979_10
ORD IDord-b591b60051dc4b9fae5e574a50a6c78b
Source noteuspto-grants-1979_10