Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1521645Generated: October 26, 2026

Tributylstannane → 5-chloro-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1521645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
ReactantEthyl AcrylateHCID 8821—
Reactant3-Chloro-2-iodoanilineHCID 21328946—
SolventDimethyl SulfoxideHCID 679—
Product5-chloro-3,4-dihydroquinolin-2(1H)-oneHCID 19027736—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a stirred solution of 3-chloro-2-iodoaniline (143-3; 1.1 g, 0.0043 mol), AIBN (0.282 g, 0.0017 mol), tributyl tinhydride (1.8 g, 0.0064 mol) in dimethyl sulphoxide (10 mL) was added ethylacrylate (1.7 g, 0.173 mol) portion wise at 0° C. Reaction mixture was allowed to stir at 120° C. for 12 h. The reaction mixture was diluted with ice cold water (150 mL) and extracted with ethyl acetate (4×100 mL). The combined organic layer was washed with saturated aqueous sodium chloride solution, dried over sodium sulphate and concentrated under vacuum to obtain the title compound. 1H NMR (400 MHz, CDCl3) δ 7.159-7.119 (t, J=7.6 Hz, 1H), 7.021-7.002 (d, J=7.6 Hz, 1H), 6.819-6.800 (d, J=7.6 Hz, 1H), 2.941-2.651 (t, J=8 Hz, 4H). MS (M+1): 181.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073929B2
Source datasetuspto-grants-2015_07
ORD IDord-2f15a7fe4ec9439ea998c3a5649177e8
Source noteuspto-grants-2015_07