HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425736Generated: October 26, 2026
2,5-Dichloronitrobenzene → Escitalopram Oxalate
https://huagongshe.com/reaction/2425736
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | 4-(4-(Dimethylamino)-1-(4-fluorophenyl)-1-hydroxybutyl)-3-(hydroxymethyl)benzonitrile | HCID 10132164 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | Escitalopram Oxalate | HCID 146571 | — |
Reaction Steps
To a solution of 10 gm of (RS)-(±)4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)-benzonitrile in 50 ml of dimethylsulfoxide (DMSO) at room temperature was added 12 gm of anhydrous K2CO3 and 6.73 gm of 2,5-dichloronitrobenzene was added to the above reaction mixture at room temperature and stirred at 100° C. for 15 hours. To the reaction mixture, 250 ml of water was added and 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 40 ml of acetone at 30° C. and 3.4 gm of oxalic acid dihydrate was added to it, stirred, cooled, filtered and dried at 60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964742B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-d52c41828c40409c8475786eb9eb2aee |
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| Source note | uspto-grants-2011_06 |
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