HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1885028Generated: November 1, 2026
Oxalic Acid → N-Desmethyl Citalopram Oxalate
https://huagongshe.com/reaction/1885028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Oxalic Acid | HCID 971 | — |
| Reactant | Escitalopram Oxalate | HCID 146571 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Desmethyl Citalopram Oxalate | HCID 12371057 | — |
Reaction Steps
A solution of 1-[3-(N-methyl-ammonium)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofuran-carbonitrile (0.70 g, 2.24 mmol) and formaldehyde (0.5 mL, 6.7 mmol, 37% aqueous solution) in 98% formic acid (5 mL) was refluxed for 4 h. After cooling, 4 M HCI (2 mL) was added and the resulting mixture was evaporated. 1 M NaOH (50 mL) was added to the residue and extracted with Et2O (3×100 mL). The organic extract was washed with brine, dried and evaporated. The oxalate salt was isolated from acetone (0.22 g, 30%). DSC (open chamber), Tonset=157.73, Tpeak=160.80. The NMR-spectra were identical with those obtained from citalopram oxalate prepared in example 2. Anal. (C20H21N2O, C2H2O4, ¼ H2O) calcd. C: 63.06; H: 5.67; N: 6.69. Found C: 63.24; H: 5.65; N: 6.62.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06768011B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-bb919d120054465881ad9a6af0a7782e |
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| Source note | uspto-grants-2004_07 |
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