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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401604Erstellt: 25. Oktober 2026

Acetic Acid → 7-Fluorotryptophan

https://huagongshe.com/reaction/401604

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium HydroxideHCID 14798—
Edukt2-(7-Fluoro-1H-indol-3-ylmethyl)-2-formylamino-malonic acid diethyl esterHCID 57563301—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-FluorotryptophanHCID 1593014852%

Reaktionsschritte

A solution of 2-(7-Fluoro-1H-indol-3-ylmethyl)-2-formylamino-malonic acid diethyl ester in THF was treated with NaOH (300 mg in 10 mL water) at room temperature for 24 hr. The mixture was slowly acidified with acetic acid (5 mL) and then refluxed for 24 hr. The reaction mixture was concentrated under vacuum, and treated with dil. HCl (10 mL, 3M) and then again refluxed for ˜16 h. The reaction was allowed to cool to room temperature. The pH was adjusted to 6.0 with 2M KOH. The white solid that formed was filtered, washed with water, and dried under vacuum to give 7-fluoro-tryptophan (282 mg, 52%): mp 256-261° C., 1H NMR (500 MHz, DMSO-d6): 2.92-2.97 (dd, J=8.5 and 15 Hz, 1H), 3.25-3.29 (dd, J=4.0 and 15 Hz, 1H), 3.38-3.41 (dd, J=4.0 and 8.5 Hz, 1H), 6.87-6.96 (m, 2H), 7.25 (s, 1H), 7.37 (d, J=7.5 Hz, 1H), 11.36 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741942B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-00bd0c5c0620447892c414d223ac490b
Quellennotizuspto-grants-2014_06