HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904065Generated: October 29, 2026
Sulfuric Acid → 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane
https://huagongshe.com/reaction/1904065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4,7-Dihydro-2,2-dimethyl-1,3-dioxepin | HCID 392707 | — |
| Reactant | Tert-Butyl hypochlorite | HCID 521297 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octane | HCID 11094747 | 80% |
Reaction Steps
To an ice-cold (5°), stirred solution of the dioxepin (II) (12.81 g, 0.1 mole) in aqueous t-butanol (50%; 50 ml) adjusted to pH 6.0 with dilute sulfuric acid, was added t-butyl hypochlorite (11.3 g, 0.105 mole), while the pH was maintained at 6.0. The reaction mixture was allowed to rise to room temperature and stirred for 4 hrs with protection from light. Sodium bisulfite (200 mg) was added to the reaction mixture, followed by 50% aqueous sodium hydroxide to bring the pH to 12. The reaction mixture was heated at 100° for 1 hr and then cooled. The upper t-butanol layer was separated and the aqueous layer was extracted with t-butanol (3×20 ml). The combined organic layers were dried (Na2CO3). Solvent removal, followed by fractional distillation, gave the epoxide product (III) as a colorless oil in ≃80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04439613 |
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| Source dataset | uspto-grants-1984_03 |
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| ORD ID | ord-aa741b80156c4fc4b34cf1c2cc2cf44e |
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| Source note | uspto-grants-1984_03 |
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