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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126733Generated: October 25, 2026

Sodium hydride → HCID 20287596, compound

https://huagongshe.com/reaction/126733

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantOxalyl chlorideHCID 65578—
Reactant5-Oxo-1-cyclopentene-1-heptanoic acidHCID 78902—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20287596HCID 20287596—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 1.94 g. (0.08 mol) of sodium hydride in 100 ml. of tetrahydrofuran is added with stirring under argon 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 numberUS04254036
Source datasetuspto-grants-1981_03
ORD IDord-369d883df55844a0a167904338bdb401
Source noteuspto-grants-1981_03