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HRID 2061336作成日:2026年10月27日

Diethyl 1-benzylazetidine-3,3-dicarboxylate → [1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanol

https://huagongshe.com/reaction/2061336

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl 1-benzylazetidine-3,3-dicarboxylateHCID 11483175—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒TetrahydrofuranHCID 8028—
生成物AmmoniaHCID 222—
生成物[1-Benzyl-3-(hydroxymethyl)azetidin-3-YL]methanolHCID 20164320126.6%

反応手順

LiAlH4 (1.0 M in THF, 65 mL, 65 mmol) was added dropwise to a solution of diethyl 1-benzylazetidine-3,3-dicarboxylate (1.0 g, 3.43 mmol) in THF (20 mL). The resulting suspension was stirred overnight at room temperature, quenched with water (0.25 mL), 15% aq. NaOH (0.25 mL), and water (0.75 mL), filtered through celite, and concentrated in vacuo. Chromatography (7N NH3 in MeOH/CH2Cl2=5:95→10:90) of the resulting residue afforded 4 (450 mg, 63%) as an oil. 1H NMR (CDCl3): δ 7.33-7.20 (m, 5H), 3.74 (s, 4H), 3.65 (s, 2H), 3.12 (s, 4H). 13C NMR (CDCl3): δ 137.4, 129.02, 128.8, 127.7, 66.8, 63.3, 58.7, 41.0. HRMS for C12H17NO2 [M+] calcd, 207.1259; found, 207.1259.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08283345B2
出典データセットuspto-grants-2012_10
ORD IDord-e1f3af940cbb490daf67724a98e098ef
出典メモuspto-grants-2012_10