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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990652Generated: October 29, 2026

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

https://huagongshe.com/reaction/990652

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 numberUS06462032B1
Source datasetuspto-grants-2002_10
ORD IDord-b8b1b05ddd0e48a39ef0f348b36987d9
Source noteuspto-grants-2002_10