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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246735Generated: November 1, 2026

Benzyl Bromide → 1-Benzyl-3,3-dimethylindoline-2-one

https://huagongshe.com/reaction/2246735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant3,3-Dimethyl-1,3-dihydro-indol-2-oneHCID 313100—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-3,3-dimethylindoline-2-oneHCID 1108621983.1%

Reaction Steps

3,3-Dimethyl-1,3-dihydro-indol-2-one (5.5 g, 34 mmol) was dissolved in dimethylformamide (50 mL) and sodium hydride (1.4 g, 38 mmol) was added portionwise and the mixture was stirred 30 minutes then benzyl bromide (4.8 mL, 41 mmol) was added. The mixture was stirred 2 hours then quenched with saturated aqueous ammonium chloride, diluted with ether, washed with water, and saturated brine. The organic layer was separated, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude product was purified via Isco chromatography (Redisep, silica, gradient 0-20% ethyl acetate in hexane) to afford 7.1 g (83%) of 1-benzyl-3,3-dimethyl-1,3-dihydro-2H-indol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687529B2
Source datasetuspto-grants-2010_03
ORD IDord-894d1994d8e14948867ad1e7144cc5b8
Source noteuspto-grants-2010_03