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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1270436Erstellt: 25. Oktober 2026

Triethylamine → Ether methanol ammonium hydroxide

https://huagongshe.com/reaction/1270436

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
EduktN-(2-bromoethyl)methanesulfonamideHCID 285330—
LösungsmittelDimethylformamideHCID 6228—
ProduktEther methanol ammonium hydroxideHCID 13172633026%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of compound (AFD) (0.40 mmol) in dry DMF was added triethylamine (0.45), followed by the alkylating agent Br(CH2)2NHSO2CH3 (0.45 mmol). The resulting mixture was stirred at 80° C. overnight. After completion of the reaction, the cooled mixture was poured into 1M NaOH (150 mL) and extracted with ethyl acetate (2×100 mL). The organic extracts were dried (MgSO4) and the solvent evaporated at the rotary evaporator to leave a gum. Flash chromatography of the residue (SiO2, ether:methanol:ammonium hydroxide (200:10:1)) provided compound (AFV) as a colorless gum: (yield:26%); purity >97% (HPLC); MS: m/z 616.3 (M+1); 1H NMR (DMSO d6): δ 2.1–2.2 (br s, 3H), 2.3–2.4 (m, 5H), 2.75 (s, 3H) 2.9–2.10 (br s, 3H), 3.3–3.4 (m, 6H), 3.5 (m, 3H), 4.65 (m, 2H), 7.15–7.5 (m, 16H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07202259B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-7f259a7924fd41cca8357dc53868666d
Quellennotizuspto-grants-2007_04