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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427751Generated: October 30, 2026

Ethyl Acetate → (S)-5,7-dichloro-2-[1-(4-chloro-phenyl)-ethyl]-2,3-dihydro-isoindol-1-one

https://huagongshe.com/reaction/2427751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant(S)-(-)-1-(4-chlorophenyl)ethylamineHCID 1550852—
Reactant2-Bromomethyl-4,6-dichlorobenzoic acid methyl esterHCID 57949349—
SolventTolueneHCID 1140—
SolventHexaneHCID 8058—
Product(S)-5,7-dichloro-2-[1-(4-chloro-phenyl)-ethyl]-2,3-dihydro-isoindol-1-oneHCID 5794980035%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-Bromomethyl-4,6-dichloro-benzoic acid methyl ester (0.119 g, 0.4 mmol), (S)-1-(4-chloro-phenyl)-ethyl amine (0.067 mL, 0.48 mmol), and K2CO3 (0.104 g, 0.8 mmol) in toluene (5 mL) was heated with stirring at 100° C. for 2 h. Workup and silica gel column chromatography of the product using 30% ethyl acetate in hexane afforded (S)-5,7-dichloro-2-[1-(4-chloro-phenyl)-ethyl]-2,3-dihydro-isoindol-1-one (0.047 g, 35%). 1H NMR (300 MHz, CDCl3): δ (ppm) 1.64 (d, 3H), 3.94 (d, 1H), 4.26 (d, 1H), 5.74 (q, 1H) 7.22-7.42 (m, 6H). GC-MS: m/z 340 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968570B2
Source datasetuspto-grants-2011_06
ORD IDord-ad45390c1a4445a08017dbe1bd817914
Source noteuspto-grants-2011_06