HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1470106Erstellt: 25. Oktober 2026
Sodium borohydride → N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)-1-hydroxyethyl)phenyl)acetamide
https://huagongshe.com/reaction/1470106
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)acetyl)phenyl)acetamide | HCID 12149183 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)-1-hydroxyethyl)phenyl)acetamide | HCID 12149184 | — |
Reaktionsschritte
Into a 100-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)acetyl)phenyl)acetamide (1.5 g, 4.11 mmol, 1.00 equiv) in methanol (20 mL). This was followed by the addition of NaBH4 (300 mg, 7.89 mmol, 2.06 equiv) in several batches at 0-5° C. The resulting solution was stirred for 2 h at 0-5° C. The reaction was then quenched by the addition of 5 mL of acetone. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:10-1:5). This resulted in 1.2 g (76%) of N-(4-(2-((2,4-dichlorobenzyl)(methyl)amino)-1-hydroxyethyl)phenyl)acetamide as yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09006281B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-13f9d5f5c33d4ea2924088175ae4d7d2 |
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| Quellennotiz | uspto-grants-2015_04 |
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