Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587723Generated: October 29, 2026

4-(Bromomethyl)-1-naphthaldehyde → 4-((1,3-Dioxoisoindolin-2-yl)methyl)-1-naphthaldehyde

https://huagongshe.com/reaction/587723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)-1-naphthaldehydeHCID 10911903—
ReactantPhthalimide potassium saltHCID 24194345—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-((1,3-Dioxoisoindolin-2-yl)methyl)-1-naphthaldehydeHCID 8667518799.7%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 4-(bromomethyl)-1-naphthaldehyde (7 g, 28 mmol) in DMF (100 mL) was added potassium phthalimide (7.3 g, 39.5 mmol), and the mixture was heated at 85° C. for 2 h. The reaction mixture was cooled to ambient temperature and diluted with water (100 mL). The obtained solid was separated by filtration and dried under vacuum to afford the title compound as a white solid (8.8 g, 98%): mp 190-192° C.; 1H NMR (400 MHz, CDCl3) δ 10.39 (s, 1H), 9.25 (m, 1H), 8.41 (m, 1H), 8.10 (d, J=8.0 Hz, 1H), 7.95 (m, 4H), 7.80 (m, 4H), 7.61 (m, 4H), 5.39 (s, 2H); ESIMS m/z 316.09 ([M+H]+); IR (thin film) 1708 cm−1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226501B2
Source datasetuspto-grants-2016_01
ORD IDord-3f8ccc92d2714f92a68944ca35c8dbf0
Source noteuspto-grants-2016_01