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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422856Generated: November 2, 2026

Dimethylamine → dimethyl-(5-nitro-1H-inden-2-yl)-amine

https://huagongshe.com/reaction/1422856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantWaterHCID 962—
Reactant5-Nitro-2-indanoneHCID 1502066—
SolventTetrahydrofuranHCID 8028—
Productdimethyl-(5-nitro-1H-inden-2-yl)-amineHCID 6875298498%

Reaction Steps

To a solution of 5-nitro-2-indanone (885 mg, 5 mmol) in THF (15 mL) was added dimethylamine (2N in THF, 5 mL, 10 mmol) dropwise. The reaction mixture was stirred at r.t. for 5 h. Water was added and the reaction mixture was extracted with EtOAc. Combined organic layers were washed with water and brine and dried over Na2SO4. The concentrated crude product was filtered through a short pad of silica gel (EtOAc:hexane=1:1) and the filtrate was concentrated to give dimethyl-(5-nitro-1H-inden-2-yl)-amine as a dark red solid (1.0 g, 98%). Dimethyl-(5-nitro-1H-inden-2-yl)-amine (1.0 g, 4.9 mmol) was hydrogenated using Pd/C (10% dry, ca. 300 mg) and H2 in MeOH:THF (1:1, 30 mL) at 1 atm at r.t. for 5 h. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated. The concentrated filtrate was further purified via short silica gel column chromatography (EtOAc: MeOH=6:4) to give the title compound as a yellow solid (830 mg, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927548B2
Source datasetuspto-grants-2015_01
ORD IDord-2d5fdeadb1674138b2fa658b9a655a17
Source noteuspto-grants-2015_01