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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616479Generated: October 29, 2026

Water → 5-(5-Oxocyclopent-1-en-1-yl)pentyl acetate

https://huagongshe.com/reaction/616479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCalcium CarbonateHCID 10112—
ReactantBromineHCID 24408—
ReactantHCID 20465612HCID 20465612—
SolventCarbon TetrachlorideHCID 5943—
SolventChloroformHCID 6212—
SolventDimethylacetamideHCID 31374—
Product5-(5-Oxocyclopent-1-en-1-yl)pentyl acetateHCID 13289788—

Reaction Steps

To a well stirred mixture of 405 g. (4.05 moles of calcium carbonate, 3 l. of water, and 2.5 l. of chloroform cooled to 5° C. is added simultaneously 1016 g. (4.0 moles) of 1-acetoxy-2-(5-acetoxy-pentyl)-1-cyclopentene (Example 71) and a solution of 648 g. (4.05 moles) of bromine in 500 ml. of carbon tetrachloride at a rate to maintain a temperature below 10° C. The mixture is stirred for half an hour after addition of the ragents and the phases are then separated. The organic phase is washed with 2% sodium thiousulfate solution, water, and saturated brine, dried (MgSO4), and evaporated in vacuo to an oil. The oil is immediately added to a refluxing slurry of 500 g. (5.0 moles) of calcium carbonate in 2.5 l of N,N-dimethylacetamide under nitrogen and the mixture is then refluxed for thirty minutes. The mixture is cooled, filtered, and partitioned between water amd diethyl ether. The organic phase is washed with water and sarturated brine, dried (MgSO4), and evaporated to yield 757 g. of an oil, b.p. 116°-118° C. (0.25 mm.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04074056
Source datasetuspto-grants-1978_02
ORD IDord-8bafcb2b9a4d4febbd371853b46557ab
Source noteuspto-grants-1978_02