HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 444976Erstellt: 25. Oktober 2026
4-Formylbenzoic acid → 4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acid
https://huagongshe.com/reaction/444976
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Formylbenzoic acid | HCID 12088 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | Tert-butyl 3-aminopropanoate hydrochloride | HCID 16218890 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-[(2-tert-Butoxycarbonylethylamino)methyl]benzoic acid | HCID 59687909 | — |
Reaktionsschritte
Tert-butyl 3-aminopropanoate hydrochloride (5 g, 27.7 mmol) was dissolved in methanol (150 mL). Diisopropylethylamin (4.73 mL, 27.7 mmol) was added followed by 4-carboxybenzaldehyd. The mixture is heated to reflux for 1 hour. After cooling to room temperature sodium cyanoborohydride (1.77 g, 22.1 mmol) was added under nitrogen and stirred for 1 hour at room temperature. Acetic acid (15 mL) was added and the mixture was stirred for an additional 1 hour. The mixture was poured into water (300 mL) and stirred at room temperature over night. The water solution was washed with ethyl acetate (3×250 mL). The organic phase dried (Na2SO4) and solvent removed in vacuo to yield the crude product as an oil which solidifies by standing. The crude product was used in the next step without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08476228B2 |
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| Quelldatensatz | uspto-grants-2013_07 |
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| ORD ID | ord-529bb2850dd94b4484bee76555c5f515 |
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| Quellennotiz | uspto-grants-2013_07 |
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