HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 76159Erstellt: 25. Oktober 2026
Hydroxyamfetamine → Acetamide, N-[2-(4-hydroxyphenyl)-1-methylethyl]-
https://huagongshe.com/reaction/76159
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydroxyamfetamine | HCID 3651 | — |
| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | Acetamide, N-[2-(4-hydroxyphenyl)-1-methylethyl]- | HCID 584229 | — |
Reaktionsschritte
1.88 g (10.0 mmol) 4-(2-amino-propyl)-phenol*HCl and 1.80 g (21.0 mmol) NaHCO3 are combined in 50 mL water and cooled down to 0° C. 0.95 mL (10.0 mmol) acetic anhydride, dissolved in 50 mL ACN, are dropped into the mixture over a period of 1.5 h. The reaction mixture is stirred at r.t. for 72 h. The ACN is evaporated in vacuo and the aq. residue is acidified with HCl (1N). The mixture is extracted several times with EtOAc. The organic layers are combined, dried with Na2SO4 and the solvent is removed in vacuo. The crude product is purified by column chromatography (silica gel, DCM/MeOH 95/5).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835472B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-b0e8197c822641c39eb4e1d339b0eda3 |
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| Quellennotiz | uspto-grants-2014_09 |
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