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HRID 376809作成日:2026年10月26日

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

https://huagongshe.com/reaction/376809

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
反応物8-(Aminomethyl)naphthalene-2-carboxylic acidHCID 14756563—
溶媒TetrahydrofuranHCID 8028—
生成物N-(BOC)-8-aminomethyl-2-naphthoic acidHCID 1475656561.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06022523
出典データセットuspto-grants-2000_02
ORD IDord-ff8ae35276ae456385f10cbf06943b3c
出典メモuspto-grants-2000_02