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HRID 242659作成日:2026年10月27日

Acetaldehyde → Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/242659

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物(R)-(+)-1-Boc-3-aminopyrrolidineHCID 854070—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylateHCID 20800658—

反応条件

温度80 °C

反応手順

To a solution of (R)-3-amino-1-N-Boc pyrrolidine (1 eq, 5.37 mmol) in methanol (20 mL) was added acetaldehyde (0.95 eq) and the resulting mixture was heated to 80° C. and stirred for 2 h., then stirred at room temperature overnight. Sodium borohydride (0.95 eq, 5.1 mmol) was added and reaction mixture was stirred for an additional 2 h. The reaction mixture was concentrated, dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The combined organics were washed with brine and dried over sodium sulfate. The crude product was purified on silica using hexane/ethyl acetate (10%) to hexane/ethyl acetate (50%). 1H-NMR (CDCL3) δ: 1.05 (3H, t), 1.45 (9H, s), 1.60-1.75 (1H, m), 2.00-2.10 (1H, m), 2.68 (4H, q), 2.90-3.15 (1H, m), 3.25-3.65 (4H, m). ESI-MS m/z: 215 (M+1), UV retention time: 0.75 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653096B2
出典データセットuspto-grants-2014_02
ORD IDord-6de36c0f01444b1d873210d6f2fcf513
出典メモuspto-grants-2014_02