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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370306Generated: November 1, 2026

Bromine → 5-Bromo-3,3-diethyl-1,3-dihydro-2H-indol-2-one

https://huagongshe.com/reaction/1370306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium AcetateHCID 517045—
Reactant3,3-diethyl-2,3-dihydro-1H-indol-2-oneHCID 15153221—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product5-Bromo-3,3-diethyl-1,3-dihydro-2H-indol-2-oneHCID 21986250—

Reaction Steps

A solution of 3,3-diethylindol-2-one (8 g, 40 mmol) and sodium acetate (4 g, 48 mmol) in acetic acid (100 ml) was treated with bromine (6.4 g, 40 mmol). After 30 min. the mixture was diluted with water and extracted with EtOAc (2×); the combined organic layers were washed with water, sat. sodium hydrogen carbonate solution, then brine, dried (MgSO4) and evaporated-to afford the crude product (7.6 g, 75%). A sample was recrystallized from EtOAc/hexane to obtain 5-bromo-1,3-dihydro-3,3-diethyl-[2H]-indol-2-one, m. p. 164-165° C.; 1H-NMR (DMSO-d6) δ 10.45 (s, 1H), 7.41-7.40 (d, 1H, J=2.2 Hz), 7.34-7.31 (m, 1H), 6.78-6.76 (d, 1H, J=8.2 Hz), 1.78-1.65 (m, 4H), 0.50-0.46 (m, 6H); MS (−ESI) m/z 266/268 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583145B1
Source datasetuspto-grants-2003_06
ORD IDord-f183ec9f70c84aaea810522d1a2dda45
Source noteuspto-grants-2003_06