HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853717Generated: October 30, 2026
3-Chloro-N,N-dimethyl-1-propanamine → Citalopram
https://huagongshe.com/reaction/853717
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Reactant | 1-(4'-Fluorophenyl)-1,3-DihydroIsobenzofuran-5-Carbonitrile | HCID 9856159 | — |
| Product | Citalopram | HCID 2771 | — |
Reaction Steps
According to the present invention, the alkylation of 1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile (5-cyanophthalane) with N,N-dimethylaminopropylchloride may be carried out following prior art procedure, and preferably as described in U.S. Pat. No. 4,136,193. However, according to the process described in U.S. Pat. No. 4,136,193, after the completion of the alkylating reaction, the reaction mass is diluted with ice cold water and the aqueous layer is extracted into ether. The ether layer is then extracted with 20% aqueous acetic acid. The pH of the aqueous acidic layer is then adjusted to alkaline, e.g. pH 10-11, with sodium hydroxide and the citalopram base extracted into ether. The ether layer is then concentrated under reduced pressure to obtain citalopram base oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07255741B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-32215a707e114a3689476b0602d4a2ef |
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| Source note | uspto-grants-2007_08 |
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