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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661943Generated: November 4, 2026

Hydrogen Peroxide → HCID 59375146, compound

https://huagongshe.com/reaction/661943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 86642953HCID 86642953—
SolventMethanolHCID 887—
ProductHCID 59375146HCID 59375146—

Reaction Steps

Step 2 A solution of crude 4-(2-fluorophenyl)-7-formyl-9H-carbazole-1-carboxamide (25.2 mg, 0.076 mmol) in methanol (2 mL) at 0° C. was treated with 30% aqueous hydrogen peroxide (0.039 mL, 0.379 mmol) and sulfuric acid (0.020 mL, 0.379 mmol). After 1.5 h, additional hydrogen peroxide (0.100 mL) and sulfuric acid (0.050 mL) were added and the mixture was stirred at rt overnight. After 16 h, 1 M aqueous sodium hydroxide (2 mL) was added and the mixture was stirred for 1 h. The pH was adjusted to ca. 4 and the organic solvent was removed under vacuum. The aqueous residue was diluted with water and the precipitate was collected by filtration, washed with water and dried. The residue was purified by preparative HPLC to provide 4-(2-fluorophenyl)-7-hydroxy-9H-carbazole-1-carboxamide as tan solid after lypholization (5.1 mg, 21%). 1H NMR (400 MHz, methanol-d4) δ 7.81 (1H, d, J=7.70 Hz), 7.45-7.64 (2H, m), 7.21-7.42 (2H, m), 7.03 (1H, d, J=7.92 Hz), 6.90-6.99 (2H, m), 6.45 (1H, dd, J=8.58, 2.20 Hz). Mass spectrum m/z 321.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084620B2
Source datasetuspto-grants-2011_12
ORD IDord-842899c254574e248980c4ce3e2b8e49
Source noteuspto-grants-2011_12