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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1349576Generated: November 1, 2026

Aniline → HCID 21092855, compound

https://huagongshe.com/reaction/1349576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 21092938HCID 21092938—
SolventDichloromethaneHCID 6344—
ProductHCID 21092855HCID 2109285524.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a chilled solution of (4-hydroxy-2,2-dimethyl-3,4-dihydro-2H-quinolin-1-yl)-(3-methoxy-phenyl)-methanone (500 mg, 1.6 mmol) in 10 ml dichloromethane was added slowly 0.8 ml iodotrimethylsilane (5.6 mmol) at 0° C. The resulting reaction mixture was stirred at 0° C. for 6 hours. Then the mixture was concentrated under vacuum. The residue was dissolved in 12 ml TIF. BaCO3 (630 mg, 3.2 mmol) and aniline (0.17 ml, 1.92 mmol) was added. The mixture was stirred at RT overnight. The mixture was filtered and the filtrate was concentrated under vacuum. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexane (1:4) to give (2,2-dimethyl-4-phenylamino-3,4-dihydro-2H-quinolin-1-yl)-(3-methoxy-phenyl)-methanone (150 mg, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211672B2
Source datasetuspto-grants-2007_05
ORD IDord-1adde041fedb43d5a8033a196b1577d7
Source noteuspto-grants-2007_05