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HRID 1744413作成日:2026年10月24日

2-Propenoic acid, 2-(acetyloxy)-, methyl ester → (S)-methyl 2-methylcarbonyloxypropanoate

https://huagongshe.com/ja/reaction/1744413

反応式

関与物質

役割名称HCID仕込み量
反応物2-Propenoic acid, 2-(acetyloxy)-, methyl esterHCID 11137277—
反応物HCID 178418361HCID 178418361—
溶媒MethanolHCID 887—
溶媒DiphosphaneHCID 139283—
溶媒Bis(norbornadiene)rhodium(I) tetrafluoroborateHCID 10915722—
生成物(S)-methyl 2-methylcarbonyloxypropanoateHCID 11051803—

反応手順

In a 50 ml Schlenk vessel, Rh(nbd)2BF4 (5.2 mg, 1 mol %) and the diphosphine ligand (1 mol %) were dissolved in MeOH (10 ml) under argon. After all of the rhodium complex had gone into solution, methyl 2-acetoxyacrylate (200 mg, 1.39 mmol) was added. The Schienk vessel was subsequently connected via a three-way stopcock with a hydrogen balloon and an oil pump and the inert gas atmosphere was replaced by hydrogen. The reaction mixture was stirred at room temperature for 20 h and the solvent was then distilled off in an oil pump vacuum. The residue was purified by bulb tube distillation. The ester (S)-8 was obtained as a colorless oil in quantitative yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07015342B2
出典データセットuspto-grants-2006_03
ORD IDord-0489fe46fcc448b680af3d1bea2f9f8d
出典メモuspto-grants-2006_03