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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Reactant | 2-Iodoethyl ether | HCID 3430779 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Spiro[indole-3,4'-oxan]-2(1H)-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08173655B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-0f4efaa020a5402b9af1a371bdd47925 |
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| Source note | uspto-grants-2012_05 |
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