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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669966Generated: October 25, 2026

2,5-Dichloronitrobenzene → Escitalopram

https://huagongshe.com/reaction/1669966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-DichloronitrobenzeneHCID 6977—
ReactantPotassium CarbonateHCID 11430—
ReactantOxalic acid dihydrateHCID 61373—
ReactantCitadiol, (S)-HCID 7472057—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductEscitalopramHCID 146570—
ProductEscitalopram OxalateHCID 146571—

Reaction Conditions

Temperature102.5 °C

Reaction Steps

To a solution of 54.5 kg of (S)-(−)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)benzonitrile in 255 lit DMSO was added 66.0 kg of anhydrous K2CO3 and 36.7 kg of 2,5-dichloronitrobenzene at room temperature and stirred for 16 hours at 100-105° C. To the reaction mixture 2550 lit of water was added at about 30° C. The reaction mixture was extracted with toluene, the toluene layer was washed with water and 5% sodium hydroxide solution and after acid base treatment yielded an oily product. The oil was dissolved in 435 lit IPA at 30° C. and 17.7 kg of oxalic acid dihydrate was added to it, heated to 70-75° C., stirred and charcolized the clear solution, cooled, The filtrate was cooled to 5-10° C. slowly and the resultant solid was filtered, dried at 60° C. and micronised to get the oxalic acid salt of (S)-(+)-1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofuran carbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07989645B2
Source datasetuspto-grants-2011_08
ORD IDord-280ea5b9733447c6b9bc962dda2136d2
Source noteuspto-grants-2011_08