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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096957Generated: October 26, 2026

N,N,N',N'-Tetramethylethylenediamine → 6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-one

https://huagongshe.com/reaction/2096957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1,4-DiiodobutaneHCID 12337—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-oneHCID 1271709045.6%

Reaction Conditions

Temperature-20 °C

Reaction Steps

n-Butyl lithium (2.5 M in hexanes, 3.8 mL, 9.5 mmol) was added dropwise over 30 minutes to a stirred suspension of 6-bromoindolin-2-one (preparation 1, 1.00 g, 4.7 mmol) and N,N,N′,N′-tetramethylethylenediamine (1.42 mL, 9.4 mmol) in tetrahydrofuran (20 mL) at −78° C. The mixture was stirred for 1 hour, then 1,4-diiodobutane (3.11 mL, 23.6 mmol) was added dropwise over 5 minutes. The mixture was warmed to −20° C. over a 1 hour period, was stirred for a further hour at this temperature and was then warmed to room temperature. After 3 hours stirring at room temperature, saturated aqueous ammonium chloride solution was added to the reaction and the mixture was extracted with ethyl acetate. The organic layer was washed with water, brine, dried (MgSO4) and evaporated. Purification of the residue by flash chromatography (10:1 hexanes/ethyl acetate) gave the title compound (0.57 g, 45%) as a pale pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450341B2
Source datasetuspto-grants-2013_05
ORD IDord-4e9641845ee34b83a1e636ba7d59c737
Source noteuspto-grants-2013_05