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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(2-Iodoethoxy)benzeneHCID 18551759—
Reactant4,6,6a,8,9,10a-Hexahydro-10a-methylindolo[3,4-gh][1.4]benzoxazineHCID 19372778—
SolventDimethylformamideHCID 6228—
Product4,6,6a,8,9,10a-Hexahydro-10a-methyl-7-(2-phenoxyethyl)-7H-indolo[3,4-gh][1.4]benzoxazineHCID 1937279246%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466689
Source datasetuspto-grants-1995_11
ORD IDord-ad9a8e3735d6468eb043dfbcd8ad185e
Source noteuspto-grants-1995_11