HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 406401Erstellt: 26. Oktober 2026
Acetic Acid → Ethyl 5-[bis(cyclopropylmethyl)amino]-2-chlorobenzoate
https://huagongshe.com/reaction/406401
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Edukt | Ethyl 5-amino-2-chlorobenzoate | HCID 13226857 | — |
| Edukt | Borane;2-methylpyridine | HCID 16217944 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Ethyl 5-[bis(cyclopropylmethyl)amino]-2-chlorobenzoate | HCID 66618819 | — |
Reaktionsschritte
To the mixture of ethyl 5-amino-2-chlorobenzoate, cyclopropanecarboxaldehyde (458 μl) and acetic acid (1.43 ml) dissolved in methanol (20 ml), α-picoline borane (804 mg) was added at ice cool temperature, and was stirred under nitrogen atmosphere overnight at room temperature. After the reaction mixture was concentrated under reduced pressure, sodium hydrogencarbonate aqueous solution was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography, and ethyl 2-chloro-5-(cyclopropylmethylamino)benzoate (881 mg) and ethyl 5-[bis(cyclopropylmethyl)amino]-2-chlorobenzoate (423 mg) were obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08754100B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-e99f442c967e4504a62d699bd68558a7 |
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| Quellennotiz | uspto-grants-2014_06 |
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