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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921206Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → Spiro[indole-3,4'-oxan]-2(1H)-one

https://huagongshe.com/reaction/1921206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantOxindoleHCID 321710—
Reactant2-Iodoethyl etherHCID 3430779—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductSpiro[indole-3,4'-oxan]-2(1H)-oneHCID 39240582—

Reaction Steps

Butyllithium (2.5 M in hexanes, 3.76 mL, 9.39 mmol) was added to a solution of oxindole (500 mg, 3.76 mmol) at −78° C. in THF (40 mL). After complete addition, N,N,N′,N′-tetramethylethane-1,2-diamine (1.48 mL, 9.76 mmol) was added, maintaining the internal temperature <−70° C. After 1 h at −78° C., 2-iodoethyl ether (4.90 g, 15.0 mmol) was added and the reaction warmed to ambient temperature. After 48 h the reaction was quenched with H2O (5 mL) and the mixture was partitioned between EtOAc (100 mL) and H2O (100 mL). The aqueous solution was extracted with EtOAc (3×50 mL) and the combined organic layers were washed with brine (20 mL), dried over Na2SO4, filtered, and concentrated in vacuo. Purification by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 97:3, gave the title compound. MS: m/z=204 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173655B2
Source datasetuspto-grants-2012_05
ORD IDord-0f4efaa020a5402b9af1a371bdd47925
Source noteuspto-grants-2012_05