戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2238392作成日:2026年10月27日

tert-Butanol → Tert-butyl 6-cyano-2-naphthylcarbamate

https://huagongshe.com/reaction/2238392

反応式

関与物質

役割名称HCID仕込み量
反応物tert-ButanolHCID 6386—
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物6-Cyanonaphthalene-2-carboxylic acidHCID 12433090—
生成物Tert-butyl 6-cyano-2-naphthylcarbamateHCID 4454952974%

反応手順

A suspension of 6-cyano-2-naphthoic acid [J. Med. Chem., 2004, 47, 303-324] (139) (4.62 g, 23.4 mmol) in dry t-BuOH (120 mL) containing powdered molecular sieves (2 g) was treated with Et3N (3.91 mL, 28.1 mmol) and the mixture was stirred at room temperature under N2 for 30 min. DPPA (5.55 mL, 25.8 mmol) was added, and the mixture was stirred at reflux for 6 h, then concentrated to half volume and poured into dilute aqueous NaHCO3. The resulting solid was purified by chromatography on silica gel, eluting with CH2Cl2, to give tert-butyl 6-cyano-2-naphthylcarbamate (140) (4.68 g, 74%): mp (MeOH/H2O) 135-136° C.; 1H NMR [(CD3)2SO] δ 9.85 (s, 1H), 8.42 (d, J=0.9 Hz, 1H), 8.23 (d, J=1.0H, 1H), 7.95 (d, J=8.7H, 2H), 7.68 (dd, J=8.5, 1.6 Hz, 1H), 7.64 (dd, J=9.0, 2.0 Hz, 1H), 1.52 (s, 9H). Anal. (C16H16N2O2) C, H, N.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07718688B2
出典データセットuspto-grants-2010_05
ORD IDord-3e552ca8e3894f208b57401cbecdf0ca
出典メモuspto-grants-2010_05