Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 22857194 | HCID 22857194 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22857197 | HCID 22857197 | 50% |
Reaction Steps
To a solution of trans-4,6,6a,7,9,10a-hexahydro-10a-methyl-1-(2,4,6-triisopropylphenylsulfonyl)-indolo[3,4-gh][1.4]benzoxazin-8-one (220 mg, 0.43 mmol) in THF (10 ml) was added, while stirring under ice-cooling, LAH (3 equivalents). The mixture was heated for 3 hours under reflux. After completion of the reaction, ethanol was added to the reaction mixture to inactivate the excess amount of LAH. The reaction mixture was added to an ice-cooled saturated aqueous solution of Na2SO4, followed by extraction with ethyl acetate. The extract solution was washed with an aqueous saline solution, followed by drying (anhydrous Na2SO4). The solvent was distilled off under reduced pressure. The residue was subjected to a silica gel column chromatography, eluting with n-hexane-ethyl acetate (1:5), to afford 106 mg (50%) of the title compound as a syrupy 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-afcdb717072d4f678bcd6e5b4e3997b3 |
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| Source note | uspto-grants-1995_11 |
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