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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1508724Erstellt: 25. Oktober 2026

4-Aminobenzenepropanol → HCID 74221498, Verbindung

https://huagongshe.com/reaction/1508724

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-AminobenzenepropanolHCID 220424—
EduktHCID 90111613HCID 90111613—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelSodium BicarbonateHCID 516892—
ProduktHCID 74221498HCID 7422149835,4%

Reaktionsbedingungen

Temperatur75 °C

Reaktionsschritte

2-Chloro-4-(3-chlorophenyl)-6-ethyl-1,3,5-triazine (0.150 g, 0.59 mmol) and 3-(4-aminophenyl)propan-1-ol (0.130 g, 0.89 mmol) were suspended in acetic acid (5 mL). The mixture was heated to 75° C. for 2 h. After this time, the reaction was cooled, diluted with saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.077 g, 35%) as a yellow solid. MW=368.86. 1H NMR (DMSO-d6, 500 MHz) δ 10.19 (s, 1H), 8.41-8.31 (m, 2H), 7.71-7.67 (m, 3H), 7.60 (t, J=8.0 Hz, 1H), 7.24-7.16 (m, 2H), 4.45 (t, J=5.5 Hz, 1H), 3.43 (q, J=5.5 Hz, 2H), 2.77 (q, J=7.5 Hz, 2H), 2.60 (t, J=7.5 Hz, 2H), 2.51-2.49 (m, 2H), 1.75-1.69 (m, 2H), 1.32 (t, J=7.5 Hz, 3H); APCI MS m/z 369 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09221843B2
Quelldatensatzuspto-grants-2015_12
ORD IDord-5d60009078ae45ffa621d7e40dd16487
Quellennotizuspto-grants-2015_12