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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1417910Erstellt: 26. Oktober 2026

Triethylamine → N-(BOC)-8-aminomethyl-2-naphthoic acid

https://huagongshe.com/reaction/1417910

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
Edukt8-(Aminomethyl)naphthalene-2-carboxylic acidHCID 14756563—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(BOC)-8-aminomethyl-2-naphthoic acidHCID 1475656568%

Reaktionsschritte

A solution of 8-aminomethyl-2-naphthoic acid (0.50 g, 0.00025 mol) and triethylamine (0.038 mL, 0.028 g, 0.000275 mol) in aqueous tetrahydrofuran (50%, 5 mL) was added, portionwise as a solid, 2-(tert-butoxycarbonyloxyimino)-2-phenylacetonitrile (0.068 g, 0.000275 mol). All was stirred at ambient temperature over 5 hours. The solution was concentrated to half volume and extracted with diethylether. The aqueous layer was then acidified to a pH of 1.0 using hydrochloric acid (1N) and then extracted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure to give the title compound, N-(BOC)-8-aminomethyl-2-naphthoic acid (0.050 g, 0.00017 mol) as a white solid. mp=190°-191° C.; 1H NMR (DMSO) d 13.1 (bs, 1H), 8.8 (s, 1H), 8.0 (q, 2H, J=7.9 Hz), 7.9 (d, 1H, J=8.1 Hz), 7.6 (t, 1H, J=7.5 Hz), 7.65-7.55 (m, 2H), 4.6 (d, 2H, J=5.5 Hz), 1.4 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05879657
Quelldatensatzuspto-grants-1999_03
ORD IDord-71c8ba52dd174ec78f127d682a51d7b5
Quellennotizuspto-grants-1999_03