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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264505Generated: November 2, 2026

Bromine → 5-Bromo-spiro [cyclopentane-1,3'-[3h]indol]-2'(1'h)-one

https://huagongshe.com/reaction/1264505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1',2'-Dihydrospiro[cyclopentane-1,3'-indole]-2'-oneHCID 363343—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product5-Bromo-spiro [cyclopentane-1,3'-[3h]indol]-2'(1'h)-oneHCID 21986227105%

Reaction Steps

A solution of spiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one (0.27 g, 1.4 mmol) and sodium acetate (0.12 g, 1.46 mmol) in acetic acid (10 cm3) was treated with bromine (0.24 g, 1.51 mmol) in acetic acid (2 cm3). After 30 min. the mixture was poured into sat. sodium hydrogen carbonate solution and extracted with EtOAc (×2), the combined organic layers were washed with water, sat. sodium hydrogen carbonate solution, water, dried (MgSO4), and evaporated to give the title compound (0.37 g, 1.47 mmol, 96%) as an off-white solid which was used without further purification: 1H NMR (CDCl3) δ 1.8-2.27 (m, 8H), 6.79 (d, J=8 Hz, 1H), 7.30-7.39 (m, 2H), 8.63 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06544970B2
Source datasetuspto-grants-2003_04
ORD IDord-cb05cae10af64d06be87d3db8e339fb6
Source noteuspto-grants-2003_04