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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Calcium hypochlorite | HCID 24504 | — |
| Reactant | HCID 17857452 | HCID 17857452 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane | HCID 11094747 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04341756 |
|---|
| Source dataset | uspto-grants-1982_07 |
|---|
| ORD ID | ord-74d1c6020e4e4448961963e339dbf93e |
|---|
| Source note | uspto-grants-1982_07 |
|---|