HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2299561Generated: October 30, 2026
Benzaldehyde → N-benzyl-N-[2-(9H-carbazol-2-yloxy)]ethylamine
https://huagongshe.com/reaction/2299561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | 2-(9H-carbazol-2-yloxy)ethylamine | HCID 11085493 | — |
| Catalyst | Platinum oxide (PtO) | HCID 82844 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzyl-N-[2-(9H-carbazol-2-yloxy)]ethylamine | HCID 11267065 | — |
Reaction Steps
Benzaldehyde (9.38 g) was added to a solution of N-[2-(9H-carbazol-2-yloxy)]ethylamine (20 g; synthesized according to the process indicated in JP-A-9-249623) in methanol (500 mL). The mixture was then stirred at room temperature for 1 hour. Under an argon atmosphere, platinum oxide (1.00 g; mfd. by Wako Pure Chemical Industries) was added to the mixture, which was then stirred under a hydrogen atmosphere at atmospheric pressure for 3 hours. After replacing the atmosphere in the reaction system with argon, benzaldehyde (1.88 g) was added to the mixture, which was then further stirred under a hydrogen atmosphere at atmospheric pressure for 3 hours. After replacing the atmosphere with argon, the catalyst was filtered off and the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol and dried under reduced pressure to give the title compound (25.2 g) as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06495701B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-84ede2cca9b7401c9fd33d743064dcf9 |
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| Source note | uspto-grants-2002_12 |
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