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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(diphenylmethyl)-1H-indole-2,3-dioneHCID 1969277—
Reactant3-Fluoro-4-methoxyphenolHCID 14661613—
ReactantHCID 178418918HCID 178418918—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67357402HCID 6735740257%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916580B2
Source datasetuspto-grants-2014_12
ORD IDord-698bda693bd949f2a4b471b097c3c920
Source noteuspto-grants-2014_12