HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129235Generated: October 30, 2026
Ethyl Acetate → 4,6,6a,8,9,10a-Hexahydro-10a-methyl-7-(2-phenoxyethyl)-7H-indolo[3,4-gh][1.4]benzoxazine
https://huagongshe.com/reaction/129235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Iodoethoxy)benzene | HCID 18551759 | — |
| Reactant | 4,6,6a,8,9,10a-Hexahydro-10a-methylindolo[3,4-gh][1.4]benzoxazine | HCID 19372778 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,6,6a,8,9,10a-Hexahydro-10a-methyl-7-(2-phenoxyethyl)-7H-indolo[3,4-gh][1.4]benzoxazine | HCID 19372792 | 46% |
Reaction Steps
To a solution of 4,6,6a,8,9,10a-hexahydro-10a-methyl-7H-indolo[3,4-gh][1.4]benzoxazine (85 mg, 0.37 mmol) in DMF (5 ml) were added potassium carbonate (255 mg, 1.9 mmol) and 1-iodo-2-phenoxyethane (99 mg, 0.4 mmol). The mixture was heated at 60° C for 24 hours. After completion of the reaction, the reaction mixture was added to a mixture of ice water and ethyl acetate. The organic layer was separated, washed with a saturated aqueous saline solution and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to a silica gel column chromatography, eluting with n-hexane-ethyl acetate (2:1), to afford 59 mg (46%) of the title compound as an amorphous crystalline product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05466689 |
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| Source dataset | uspto-grants-1995_11 |
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| ORD ID | ord-ad9a8e3735d6468eb043dfbcd8ad185e |
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| Source note | uspto-grants-1995_11 |
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