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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759539Generated: October 29, 2026

Carbon Dioxide → 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane

https://huagongshe.com/reaction/1759539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactanttert-ButanolHCID 6386—
ReactantSodium HydroxideHCID 14798—
ReactantCalcium hypochloriteHCID 24504—
ReactantHCID 17857452HCID 17857452—
SolventWaterHCID 962—
Product4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octaneHCID 1109474768%

Reaction Steps

To an ice-cold (0°-5° C.), stirred solution of the dioxepin (150.0 g, 1.18 mole) in a mixture of t-butanol (250 ml) and water (150 ml) was added, during 1 hr, powdered calcium hypochlorite (59%; 150 g, 0.62 mole), portionwise, with continuous bubbling of carbon dioxide through the solution. After 30 min, aqueous 50% sodium hydroxide (160 g, 2 moles) was added and the suspension was refluxed, with stirring, using an oil bath (100°) for 1.5 hr. The mixture was filtered and the organic layer of the filtrate was separated. The aqueous layer was extracted once with t-butanol (50 ml) and the combined organic layers were washed with brine (3×20 ml). The combined washings were re-extracted once with t-butanol (50 ml). The solvent was removed from the organic layer in a Rotovapor at 70° and 100 mm. The residue was subject to fractional distillation and the product (III) was isolated as a colorless oil. (116.1 g, 68% yield) b.p. 65°-67°/5 mm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04341756
Source datasetuspto-grants-1982_07
ORD IDord-74d1c6020e4e4448961963e339dbf93e
Source noteuspto-grants-1982_07