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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1760303Generated: November 2, 2026

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

https://huagongshe.com/reaction/1760303

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 numberUS06841568B2
Source datasetuspto-grants-2005_01
ORD IDord-8d297fc0000a49b0b587ed2efa9ccfa9
Source noteuspto-grants-2005_01