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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 376809Erstellt: 24. Oktober 2026

Triethylamine → HCID 14756565, Verbindung

https://huagongshe.com/de/reaction/376809

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
Edukt8-(Aminomethyl)naphthalene-2-carboxylic acidHCID 14756563—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 14756565HCID 1475656561,8%

Reaktionsschritte

Part D--A solution of 8-aminomethyl-2-naphthoic acid (0.50 g, 0.03025 mol) and triethylamine (0.038 mL, 0.028 30 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 extraced 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
PatentnummerUS06022523
Quelldatensatzuspto-grants-2000_02
ORD IDord-ff8ae35276ae456385f10cbf06943b3c
Quellennotizuspto-grants-2000_02