HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400692Generated: October 29, 2026
1,5,6,7-Tetrahydro-4H-indol-4-one → HCID 60026304, compound
https://huagongshe.com/reaction/400692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,5,6,7-Tetrahydro-4H-indol-4-one | HCID 280229 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 57809800 | HCID 57809800 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 60026304 | HCID 60026304 | 58% |
Reaction Steps
To a suspension of 7-[1,1-dimethyl-2-(2-trifluoromethyloxiranyl)ethyl]-5-methanesulfonyl-2,3-dihydrobenzofuran (101 mg, 0.33 mmol) and 1,5,6,7-tetrahydroindol-4-one (74.9 mg, 0.56 mmol) in 0.75 mL of anhydrous ethanol was added sodium ethoxide (21 wt. % solution in ethanol, 103 μL). After heating at 85° C. for 16 hours, the reaction mixture was diluted with ethyl acetate, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified by column chromatography with silica gel (eluted with 50% to 60% ethyl acetate-hexanes) to give 80.0 mg (58% yield) of the title compound as a white solid, m.p. 207° C.-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741897B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-12c7a7db30cc441eaf0a68e5e825fbf3 |
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| Source note | uspto-grants-2014_06 |
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