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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
Reactant4,7-Dihydro-2,2-dimethyl-1,3-dioxepinHCID 392707—
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantSodium BisulfiteHCID 23665763—
Solventtert-ButanolHCID 6386—
Product4,4-Dimethyl-3,5,8-trioxabicyclo[5.1.0]octaneHCID 1109474780%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04439613
Source datasetuspto-grants-1984_03
ORD IDord-aa741b80156c4fc4b34cf1c2cc2cf44e
Source noteuspto-grants-1984_03