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HRID 5350作成日:2026年10月23日

Boron trifluoride etherate → 4-Bromo-7-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxaldehyde diethy acetal

https://huagongshe.com/ja/reaction/5350

反応式

関与物質

役割名称HCID仕込み量
反応物Boron trifluoride etherateHCID 8000—
反応物Ethyl orthoformateHCID 31214—
反応物DiisopropylethylamineHCID 81531—
反応物4-Bromo-7-methoxy-1-indanoneHCID 223379—
溶媒DichloromethaneHCID 6344—
生成物4-Bromo-7-methoxy-1-oxo-2,3-dihydro-1H-indene-2-carboxaldehyde diethy acetalHCID 10450105—

反応条件

温度0 °C

反応手順

Triethyl orthoformate (16.5 ml) was cooled to -30° C. and 15.0 ml BF3.Et2O in 50 ml methylene chloride was added. The reaction was warmed to 0° C. for 15 min, and then cooled to -78° C. To the reaction was added 12.05 g of the product from Example 34 in 50 ml methylene chloride, followed by dropwise addition of 19.4 ml diisopropyl ethyl amine. The reaction was then warmed to -15° C. for 2 h, then quenched in 5% NaHCO3 solution and extracted with methylene chloride. The organic extracts were washed with brine, dried (MgSO4), and the solvent removed. The crude product was triturated with cold hexane, and the crystalline product collected to yield 14.60 g of a white solid, mp: 76°-8° C. NMR (CDCl3) δ 1.05 (t, 3H), 1.27 (t, 3H), 3.03 (m, 2 H), 3.30 (m, 1H), 3.43-3.80 (m, 4H), 3.95 (s, 3H), 5.00 (d, 1H), 6.71 (d, 1H), 7.63 (d, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244888
出典データセットuspto-grants-1993_09
ORD IDord-0c78cd059b394bef950f6b265b6865dc
出典メモuspto-grants-1993_09