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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587252Generated: October 29, 2026

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

https://huagongshe.com/reaction/587252

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−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226500B2
Source datasetuspto-grants-2016_01
ORD IDord-21c584c36da64e9aba1cfc17b634cc7d
Source noteuspto-grants-2016_01