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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640022Generated: November 2, 2026

4-Isopropylaniline → HCID 57429432, compound

https://huagongshe.com/reaction/1640022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IsopropylanilineHCID 7464—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 2-(bromomethyl)-5-chlorobenzoateHCID 13272463—
SolventEthanolHCID 702—
ProductHCID 57429432HCID 5742943253.1%

Reaction Steps

A mixture of ethyl 2-(bromomethyl)-5-chlorobenzoate (0.553 g, 1.99 mmol), 4-isopropylaniline (0.269 g, 1.99 mmol) and sodium ethoxide (0.406 g, 5.97 mmol) in ethanol (40 mL) was heated at reflux overnight. After this time, the mixture was cooled to room temperature and concentrated under vacuum. The mixture was partitioned between 1 N HCl and ethyl acetate. The organic layer was separated, washed with 1 N HCl, then with 1:1 water/brine solution, dried over sodium sulfate and filtered. Concentration under vacuum and recrystallization from ethyl acetate afforded 6-chloro-2-(4-isopropylphenyl)isoindolin-1-one (0.302 g, 53%) as an off-white solid: m.p. 206-209° C.; 1H NMR (500 MHz, CDCl3) δ 7.89 (d, J=1.9 Hz, 1H), 7.73 (dt, J=8.6, 2.7 Hz, 2H), 7.55 (dd, J=8.1, 1.9 Hz, 1H), 7.45 (d, J=8.0 Hz, 1H), 7.30 (dt, J=8.5, 2.5 Hz, 2H), 4.83 (s, 2H), 2.96-2.90 (m, 1H), 1.26 (d, 6H); ESI MS m/z 286 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110681B2
Source datasetuspto-grants-2012_02
ORD IDord-18922b1730304cbba908a1f6ff1e29cc
Source noteuspto-grants-2012_02