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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256208Generated: October 30, 2026

Ethyl Acetate → HCID 42597939, compound

https://huagongshe.com/reaction/1256208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantHCID 66741757HCID 66741757—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventAnisoleHCID 7519—
ProductHCID 42597939HCID 42597939—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of (Z)-7-chloro-3-(3,4-diethylbenzyl)-5-(4-fluorophenyl)-1-methyl-1H-benzo[e][1,4]diazepin-2(3H)-one (0.1 g, 0.18 mmol) in anisole (3 mL) was added aluminum chloride (0.144 g, 1.08 mmol). The mixture was heated at 85° C. for 1 hour, cooled to ambient temperature and poured into a mixture of ice/water (10 mL) and ethyl acetate (20 mL) and stirred vigorously for 10 min. The layers were separated and the organic phase was dried over sodium sulfate, filtered, and then concentrated. The residue was purified by chromatography (silica gel, 95:5 CH2Cl2:MeOH) to provide an oil which was dissolved in a mixture of acetonitrile (3 mL) and water (1 mL). This solution was freeze-dried overnight to give (Z)-7-chloro-3-(3,4-diethylbenzyl)-5-(4-fluorophenyl)-1H-benzo[e][1,4]diazepin-2(3H)-one as an off-white solid: mp 88-90° C.; 1H NMR (300 MHz, DMSO-d6) δ 10.71 (s, 1H), 7.64 (dd, J=8.8, 2.5 Hz, 1H), 7.49 (t, J=5.6 Hz, 2H), 7.30-7.23 (m, 4H), 7.13-7.01 (m, 3H), 3.65 (t, J=5.5 Hz, 1H), 3.32-3.31 (m, 2H), 2.56 (quintet, J=7.3 Hz, 4H), 1.13 (q, J=7.2 Hz, 6H); APCI MS m/z 435 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461153B2
Source datasetuspto-grants-2013_06
ORD IDord-8a965b04b9724e4b966a86421cd3de19
Source noteuspto-grants-2013_06