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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1925188Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acid

https://huagongshe.com/reaction/1925188

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium CarbonateHCID 10340—
Edukt4-(Aminomethyl)Benzoic AcidHCID 65526—
EduktFmoc-N-hydroxysuccinimideHCID 21653429—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acidHCID 275608399%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To 4-aminomethyl-benzoic acid (10.6 g, 70.1 mmol) in dioxane (130 mL) was added 9% aqueous Na2CO3 (150 mL) followed by 9-fluorenylmethyloxycarbonyl-N-hydroxysuccinimide (26 g, 77 mmol). The solution was heated to 40° C. for 12 h and then cooled to room temperature. The reaction was acidified with 1 M HCl (500 mL), and extracted with ether (300 mL) to obtain acid S23 as a fluffy white solid (25.9 g, 69.4 mmol, 99%). 1H NMR (500 MHz, d6-DMSO): δ 12.85 (broad s, 1H), 7.90 (m, 4H), 7.70 (m, 2H), 7.39 (m, 2H), 7.31 (m, 4H), 4.37 (d, 2H, J=6.8 Hz), 4.24 (d, 2H, J=5.8 Hz), 4.23 (t, 1H, J=6.8 Hz). APCI/MS: 372 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08178579B2
Quelldatensatzuspto-grants-2012_05
ORD IDord-e28eb4aad354416cad5fd630f6e77115
Quellennotizuspto-grants-2012_05