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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990637Generated: October 25, 2026

Sodium Carbonate → 5-Bromo-3-methyl-indol-2-one

https://huagongshe.com/reaction/990637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBromineHCID 24408—
Reactant3-MethyloxindoleHCID 150923—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product5-Bromo-3-methyl-indol-2-oneHCID 2201937693.7%

Reaction Steps

Under an atmosphere of nitrogen, bromine (0.96 g, 6.0 mmol) in acetic acid (5 cm3). was added drop wise to a solution of 3-methyl-2-indolinone (0.8749 g, 6.0 mmol) (Kende, et al, Synth. Commun., 12, 1, 1982) and sodium acetate (0.50 g, 6.0 mmol) in acetic acid (10 cm3). The reaction was stirred at room temperature for 3.5 h. Saturated sodium carbonate was added to quench the reaction. The water layer was extracted EtOAc (×3), dried (MgSO4), filtered, and evaporated to give the title compound (1.26 g, 93%), Mp=119-120° C.; 1H NMR (DMSO) δ 1.32 (d, 3H, J=7.66 Hz), 3.45 (q, 1H, J=7.62 Hz), 6.77 (d, 1H, J=8.23 Hz), 7.46 (s, 1H), 7.36-7.33 (m, 1H), 10.4 (s, 1H); IR (KBr) 3200, 1725 cm−1; MS (EI) m/z 224/226 (M−H)−; CHN calculated for C9H8BrNO: C, 47.82; H, 3.57; N, 6.20; Found: C, 47.44; H, 3.42; N, 6.04.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06462032B1
Source datasetuspto-grants-2002_10
ORD IDord-502dabb16e32404ebd2739f1cd3b52a5
Source noteuspto-grants-2002_10