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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427575Generated: November 3, 2026

Hexane → 5-Chloro-2-(1-oxo-1,3-dihydroisoindol-2-ylmethyl)benzonitrile

https://huagongshe.com/reaction/2427575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantPhthalimidineHCID 10199—
ReactantCesium carbonateHCID 10796—
Reactant18-Crown-6HCID 28557—
Reactant2-(Bromomethyl)-4-chlorobenzonitrileHCID 12668053—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-2-(1-oxo-1,3-dihydroisoindol-2-ylmethyl)benzonitrileHCID 6725246241%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 2,3-dihydro-isoindol-1-one (0.066 g, 0.5 mmol), 2-bromomethyl-4-chloro-benzonitrile (0.116 g, 0.6 mmol), Cs2CO3 (0.408 g, 1.25 mmol), and 18-crown-6 (0.013 g, 0.05 mmol) in acetone (3 mL) was stirred at 70° C. for 16 h. Workup and silica gel column chromatography using 30% ethyl acetate in hexane afforded 5-chloro-2-(1-oxo-1,3-dihydroisoindol-2-ylmethyl)benzonitrile (0.057 g, 41%). 1H NMR (300 MHz, CDCl3): δ (ppm) 4.48 (s, 2H), 5.08 (s, 2H), 7.42-7.65 (m, 611), 7.92 (d, 1H). GC-MS: m/z 282 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-ce6e8af3aff34718b83727afe57a22c1
Source noteuspto-grants-2011_06