Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505648Generated: October 25, 2026

Water → (3R*,4R*)-3,4-epoxy-2,2-dimethyl-7-nitro-3-chromanol

https://huagongshe.com/reaction/505648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylimidazoleHCID 1390—
ReactantSodium ThiosulfateHCID 24477—
Reactant2,2-Dimethyl-7-nitro-2h-1-benzopyranHCID 13222887—
ReactantSodium HypochloriteHCID 23665760—
SolventEthyl AcetateHCID 8857—
Product(3R*,4R*)-3,4-epoxy-2,2-dimethyl-7-nitro-3-chromanolHCID 8676116266%

Reaction Steps

To a solution of 2,2-dimethyl-7-nitrobenzopyran (11.1 g, 53.9 mmol) in ethyl acetate (165 mL), (Cyc, Ph)-salen manganese complex (XX) (405 mg, 0.431 mmol) and N-methyl imidazole (858 μL, 10.8 mmol) were added, and sodium hypochlorite aqueous solution (101 g, 162 mmol) was added dropwise at 20° C. thereto over 15 minutes. After stirring the resulting mixture at room temperature for 3 hours, saturated sodium thiosulfate aqueous solution was added thereto under cooling with water. The resulting reaction solution was filtered through celite, the organic phase was washed with saturated sodium thiosulfate aqueous solution and saturated sodium chloride solution, and then dried over magnesium sulfate, and concentrated under a reduced pressure. The resulting solid was recrystallized in ethanol to obtain (3R*,4R*)-3,4-epoxy-2,2-dimethyl-7-nitro-3-chromanol (yield: 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781483B2
Source datasetuspto-grants-2010_08
ORD IDord-e392a0e5e27e458ab8bdd91aa9283013
Source noteuspto-grants-2010_08