HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154775Generated: October 30, 2026
HCID 13373177, compound → HCID 20563350, compound
https://huagongshe.com/reaction/1154775
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 13373177 | HCID 13373177 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20563350 | HCID 20563350 | — |
Reaction Steps
876 mg of potassium tert.butylate were added under a nitrogen atmosphere to a solution of 2.37 g of 1,2,3,4,5,8,8a,9,10,10a-decahydro-2,3-dimethylene-1,4-epoxy-8-mesyloxyanthracen-5-one in 40 ml of tetrahydrofuran, there being formed 1,2,3,4,9,10-hexahydro-2,3-dimethylene-1,4-epoxyanthracen-5-ol. After stirring at room temperature for 1 hour, a further 877 mg of potassium tert.butylate were added. The mixture was stirred for a further 45 minutes, 1.32 ml of methyl iodide were added and the resulting mixture was stirred for a further 1 hour. The mixture was treated with 100 ml of aqueous ammonium chloride and extracted three times with 100 ml of diethyl ether each time. After washing with three 100 ml portions of ammonium chloride solution, the combined organic phases were dried over magnesium sulphate. There were obtained 1.56 g (87%) of crude 1,2,3,4,9,10-hexahydro-2,3-dimethylene-1,4-epoxy-5-methoxyanthracene of melting point 145°-147° C. (from methanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04298535 |
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| Source dataset | uspto-grants-1981_11 |
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| ORD ID | ord-6cb1befc5c8740429e824802f0c22352 |
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| Source note | uspto-grants-1981_11 |
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