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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829058Generated: November 2, 2026

Oxindole → HCID 69662062, compound

https://huagongshe.com/reaction/1829058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxindoleHCID 321710—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant3-[(Dimethylamino)methyl]-2-benzofuran-1(3H)-oneHCID 22061504—
ReactantLiHMDS tetrahydrofuranHCID 23714775—
SolventTetrahydrofuranHCID 8028—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 69662062HCID 6966206224.4%

Reaction Steps

To a solution of oxindole (205 mg, 1.54 mmol) in dimethoxyethane (4.0 ml) at room temperature was added 1.0M LiHMDS in THF (1.54 ml). After stirring for 10 minutes at room temperature, 3-dimethylaminomethyl-3H-isobenzofuran-1-one (235 mg, 1.23 mmol) in dimethoxyethane (0.5 ml) was added and the mixture was stirred rapidly for 1 hour. Additional 1.0M LiHMDS/THF (1.54 ml) was added. After 2 hours the reaction was quenched into 10% HCl (50 ml) and 25 ml water added. The aqueous layer was washed with EtOAc and then basified with saturated NaHCO3 aqueous solution. The aqueous layer was extracted with EtOAc. The EtOAc layer was washed with brine, dried over anhydrous Na2SO4, and rotary evaporated to provide a yellow solid. The yellow solid was chromatographed silica gel column (CHCl3 to 2.5% MeOH/CHCl3 gradient) and then recrystallized from MeOH to give 3-(3-dimethylaminomethy-3H-isobenzofuran-1-ylidene)-1,3-dihydro-indol-2-one as yellow needles (92 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060844B2
Source datasetuspto-grants-2006_06
ORD IDord-b5f848af52d845f6b7f939f1b275e9ee
Source noteuspto-grants-2006_06