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HRID 260131作成日:2026年10月27日

Imidazole → Benzyl 4-(2-iodoethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/260131

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物IodineHCID 807—
反応物TriphenylphosphineHCID 11776—
反応物Benzyl 4-(2-hydroxyethyl)piperidine-1-carboxylateHCID 13971210—
生成物Benzyl 4-(2-iodoethyl)piperidine-1-carboxylateHCID 14600697—

反応条件

温度0 °C

反応手順

A solution of 3-2(263 g, 116 mmol) was treated with triphenylphosphine (33.5 g, 128 mmol), imidazole (11.9 g, 175 mmol) and cooled to 0° C. Iodine (32.4 g, 128 mmol) was added and the ice bath was removed. The reaction was filtered into a separatory funnel and the solution was washed with H2O and brine, dried over MgSO4 and concentrated. The residue was chromatographed (10% EtOAc/Hexanes) to give 3-3 as a colorless oil. Rf (20% EtOAc/Hexanes) 0.56 1H NMR (300 MHz, CDCl3) δ 7.4-7.1 (m, 5H), 5.2-5.05 (bs, 2H), 4.3-4.1 (bs, 2H), 3.2 (t, 2H), 2.8 (bs, 2H), 1.8-1.5 (m, 5H), 1.15 (m, 2H). ##STR31## 2(N-t-Butyloxycarbonylaminopiperidin-4-yl)ethanol (4-1)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05525617
出典データセットuspto-grants-1996_06
ORD IDord-c28c39753c9847c4954ff6b09d0aa8be
出典メモuspto-grants-1996_06