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HRID 1367237作成日:2026年10月25日

Diisopropylethylamine → 1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylate

https://huagongshe.com/reaction/1367237

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Benzyl succinimido carbonateHCID 83172—
反応物Methyl 4-allylpiperidine-4-carboxylateHCID 66972977—
溶媒AcetonitrileHCID 6342—
生成物1-Benzyl 4-methyl 4-allylpiperidine-1,4-dicarboxylateHCID 58893186—

反応手順

A mixture of methyl 4-allylpiperidine-4-carboxylate from Step A (5.30 g, 24.2 mmol), N-(benzyloxycarbonyloxy)succinimide (7.25 g, 29.1 mmol), and N,N-diisopropylethylamine (12.7 mL, 72.7 mmol) in CH3CN (61 mL) was stirred for 16 h. The solvent was removed in vacuo and the residue was partitioned between EtOAc (100 mL) and saturated NaHCO3 (100 mL). The organic layer was separated and the aqueous layer was further extracted with EtOAc (2×100 mL). The combined organic extracts were concentrated in vacuo to give a residue that was purified by silica gel chromatography, eluting with a gradient of hexane:EtOAc—100:0 to 40:60, to give the title compound. MS: m/z=318 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07893079B2
出典データセットuspto-grants-2011_02
ORD IDord-84147da71ee540f2a9dd29af4f9ce166
出典メモuspto-grants-2011_02