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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 66974Generated: October 29, 2026

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

https://huagongshe.com/reaction/66974

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 56) 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 reagents and the phases are then separated. The organic phase is washed with 2% sodium thiosulfate 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 and diethyl ether. The organic phase is washed with water and saturated 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 numberUS04343949
Source datasetuspto-grants-1982_08
ORD IDord-226707a293854f7fa883bbefae7c0a82
Source noteuspto-grants-1982_08