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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 2,2-Dimethyl-7-nitro-2h-1-benzopyran | HCID 13222887 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3R*,4R*)-3,4-epoxy-2,2-dimethyl-7-nitro-3-chromanol | HCID 86761162 | 66% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07781483B2 |
|---|
| Source dataset | uspto-grants-2010_08 |
|---|
| ORD ID | ord-e392a0e5e27e458ab8bdd91aa9283013 |
|---|
| Source note | uspto-grants-2010_08 |
|---|