HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712222Generated: October 25, 2026
2,5-Dichloronitrobenzene → Escitalopram Oxalate
https://huagongshe.com/reaction/1712222
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,5-Dichloronitrobenzene | HCID 6977 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxalic acid dihydrate | HCID 61373 | — |
| Reactant | Citadiol, (S)- | HCID 7472057 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | Escitalopram Oxalate | HCID 146571 | — |
Reaction Steps
To a solution of 6.0 gm of (S)-(−)-4-[4-(dimethylamino)-1-(4-fluorophenyl)-1-hydroxy-1-butyl]-3-(hydroxymethyl)-benzonitrile in 30 ml of DMSO at room temperature was added 7.3 gm of anhydrous K2CO3 and 4.04 gm of 2,5-dichloronitrobenzene was added to the above reaction mixture at room temperature and stirred at 100° C. for 15.0 hours. To the above reaction mixture, 120 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 16 ml of acetone at 30° C. and 1.9 gm of oxalic acid dihydrate in 8 ml of acetone 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 | US07790935B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-0d00751ee97c4a31a95354c5bfe00596 |
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| Source note | uspto-grants-2010_09 |
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