HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407476Generated: November 1, 2026
1-(diphenylmethyl)-1H-indole-2,3-dione → HCID 67357402, compound
https://huagongshe.com/reaction/1407476
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(diphenylmethyl)-1H-indole-2,3-dione | HCID 1969277 | — |
| Reactant | 3-Fluoro-4-methoxyphenol | HCID 14661613 | — |
| Reactant | HCID 178418918 | HCID 178418918 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67357402 | HCID 67357402 | 57% |
Reaction Steps
To a solution of 3-fluoro-4-methoxyphenol (Niemann, M. B. J. Am. Chem. Soc. (1941), 63:609) (4.60 g, 32.4 mmol) in tetrahydrofuran (60 mL) at 5° C. was added a 2 M solution of isopropylmagnesium chloride in tetrahydrofuran (18.0 mL, 36.0 mmol). Tetrahydrofuran was removed under reduced pressure and dichloromethane (60 mL) was added. To the solution was added a solution of 1-(diphenylmethyl)-1H-indole-2,3-dione (8.00 g, 25.5 mmol) in dichloromethane (60 mL) at 5° C. and the reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was quenched with saturated ammonium chloride solution (5 mL). The reaction mixture was dried over magnesium sulfate, filtered and evaporated under reduced pressure. The residue was subjected to column chromatography with 40% to 90% gradient of ethyl acetate in hexanes to afford 1-(diphenylmethyl)-3-(4-fluoro-2-hydroxy-5-methoxyphenyl)-3-hydroxy-1,3-dihydro-2H-indol-2-one (6.60 g, 57%) as a pink solid: MS (ES+) m/z 438.3 (M−17).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916580B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-698bda693bd949f2a4b471b097c3c920 |
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| Source note | uspto-grants-2014_12 |
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