HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258824Erstellt: 25. Oktober 2026
4-(Dimethylamino)benzoic acid → 1-[4-(Dimethylamino)benzoyl]-4-(diphenylmethyl)piperidine
https://huagongshe.com/reaction/258824
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-(Dimethylamino)benzoic acid | HCID 12092 | — |
| Edukt | 4-Benzhydrylpiperidine | HCID 88278 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 1-[4-(Dimethylamino)benzoyl]-4-(diphenylmethyl)piperidine | HCID 12810404 | — |
Reaktionsschritte
To a solution of 150 parts of 4-(diphenylmethyl)piperidine and 99 parts of 4-(dimethylamino)benzoic acid in 4000 parts of dichloromethane is added a solution of 123 parts of N,N1 -methanetetraylbiscyclohexanamine in 1330 parts of dichloromethane. The resultant mixture is stirred for 6 hours, whereupon a further 25 parts of 4-(dimethylamino)benzoic acid and 30 parts of N,N1 -methanetetraylbiscyclohexanamine is introduced and stirring continued thereafter for 24 hours. The reaction mixture is then filtered, and the filtrate is stripped of solvent by vacuum distillation. The residue is taken up in ether; and the ether solution is consecutively washed with 5% hydrochloric acid, water, and 5% ammonium hydroxide, then dried over anhydrous potassium carbonate and finally stripped of solvent by vacuum distillation. The residue is recrystallized from a mixture of benzene and hexane to give 1-[4-(dimethylamino)benzoyl]-4-(diphenylmethyl)piperidine melting at 177°-179°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04035372 |
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| Quelldatensatz | uspto-grants-1977_07 |
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| ORD ID | ord-dadc7376b1c94fbcb7582c200eed6207 |
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| Quellennotiz | uspto-grants-1977_07 |
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