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HRID 2096957Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/2096957

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N,N',N'-TetramethylethylenediamineHCID 8037—
Edukt1,4-DiiodobutaneHCID 12337—
EduktAmmonium ChlorideHCID 25517—
Edukt6-bromo-2,3-dihydro-1H-indol-2-oneHCID 2773289—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt6'-Bromospiro[cyclopentane-1,3'-indolin]-2'-oneHCID 1271709045,6%

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08450341B2
Quelldatensatzuspto-grants-2013_05
ORD IDord-4e9641845ee34b83a1e636ba7d59c737
Quellennotizuspto-grants-2013_05