N-Methylbutylamine → Methyl 3-bromo-5-{[butyl(methyl)amino]methyl}benzoate

HRID 348905

Reaktionsgleichung

Reaktionsgleichung von HRID 348905
[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH2:12]O)[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6].CS(Cl)(=O)=O.C(N(CC)CC)C.[CH3:26][NH:27][CH2:28][CH2:29][CH2:30][CH3:31]>C(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH:9]=[C:10]([CH2:12][N:27]([CH2:28][CH2:29][CH2:30][CH3:31])[CH3:26])[CH:11]=1)[C:5]([O:7][CH3:8])=[O:6]

Komponenten

6

Edukt 4

HCID 8068N-MethylbutylamineHCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 11356988Methyl 3-bromo-5-(hydroxymethyl)benzoate

Produkt 1

HCID 21086161Methyl 3-bromo-5-{[butyl(methyl)amino]methyl}benzoate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of methyl 3-bromo-5-(hydroxymethyl)benzoate (4.1 g, 16.8 mmol) in anhydrous methylene chloride (35 mL) at −30° C. is added methanesulfonyl chloride (1.82 mL, 23.5 mmol) followed by triethylamine (4.7 mL, 33.6 mmol). The reaction mixture is stirred for 45 min at 0° C., and then filtered. The filtrate is added to N-methylbutylamine (6 mL, 50.4 mmol) and stirred at room temperature for 16 h. The solution is concentrated under reduced pressure, and the residue is purified by flash column chromatography (silica, 8% ethyl acetate/hexanes) to give the title compound. ESI MS m/z 314.1 [M+H]+.

Aufarbeitung

  1. filtrationfiltered
  2. stirringstirred at room temperature for 16 h
  3. concentrationThe solution is concentrated under reduced pressure
  4. customthe residue is purified by flash column chromatography (silica, 8% ethyl acetate/hexanes)

Quellen und Nachweise

ORD-Eintrag
ord-873971a8181848428c5d44942988e7a1
Quelldatensatz
uspto-grants-2007_02
Patentnummer
US07176242B2

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