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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | 4-(Aminomethyl)Benzoic Acid | HCID 65526 | — |
| Edukt | Fmoc-N-hydroxysuccinimide | HCID 21653429 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 4-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acid | HCID 2756083 | 99% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08178579B2 |
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| Quelldatensatz | uspto-grants-2012_05 |
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| ORD ID | ord-e28eb4aad354416cad5fd630f6e77115 |
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| Quellennotiz | uspto-grants-2012_05 |
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