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 | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Escitalopram | HCID 146570 | — |
| Product | Escitalopram Oxalate | HCID 146571 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989645B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-280ea5b9733447c6b9bc962dda2136d2 |
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| Source note | uspto-grants-2011_08 |
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