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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1682523Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/1682523

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

Part D--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
PatentnummerUS05635477
Quelldatensatzuspto-grants-1997_06
ORD IDord-8269a50782af465791644a8f5537c027
Quellennotizuspto-grants-1997_06