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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306567Generated: October 30, 2026

Triethylsilane → 5,6-dihydro-5-oxo-11H-indeno [1,2-c]isoquinoline

https://huagongshe.com/reaction/2306567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylsilaneHCID 12052—
ReactantHCID 13802540HCID 13802540—
ReactantDichloromethane methanolHCID 21226129—
SolventTrifluoroacetic acidHCID 6422—
Product5,6-dihydro-5-oxo-11H-indeno [1,2-c]isoquinolineHCID 1010538888.7%

Reaction Steps

To a stirred suspension of 2 (40 g, 0.16 mol) in trifluoroacetic acid (2.5 L) was added triethylsilane (94 g, 0.8 mol) in small portions at room temperature and the reaction mixture was stirred for 96 h, during which time the reaction progress was monitored using TLC (eluent −5% MeOH/CH2Cl2). The reaction mixture was slowly poured on ice, filtered, washed with copious amounts of H2O and MeOH and dried in vacuo to provide the above-titled compound 6 (33.1 g, 88%), whose spectral data were identical to those of a sample of compound 6 that was obtained using Method I.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828319B2
Source datasetuspto-grants-2004_12
ORD IDord-bd79d371148a42329cb390f2c6c3bd85
Source noteuspto-grants-2004_12