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HRID 535048作成日:2026年10月26日

Toluene → 2-benzyl 3-methyl (2S,3S,5R)-1-benzyl-5-(1-ethoxyethoxy)piperidine-2,3-dicarboxylate

https://huagongshe.com/reaction/535048

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物1-benzyl 4-methyl(2S)-2-[benzyl((2S)-2-(1-ethoxyethoxy)-3-[(4-methylphenyl)sulfony]oxypropyl)amino]succinateHCID 87348497—
溶媒TetrahydrofuranHCID 8028—
生成物2-benzyl 3-methyl (2S,3S,5R)-1-benzyl-5-(1-ethoxyethoxy)piperidine-2,3-dicarboxylateHCID 13173192569.9%

反応条件

温度-78 °C

反応手順

To a solution of 1-benzyl 4-methyl (2S)-2-[benzyl((2S)-2-(1-ethoxyethoxy)-3-[(4-methylphenyl)sulfonyl]oxypropyl)amino]succinate (35.7 g, 0.0569 mol) in a mixture of tetrahydrofuran (95.5 mL, 1.18 mol) and toluene (490 mL, 4.6 mol) at −78 Celsius was added 1.00 M of Lithium hexamethyldisilazide in tetrahydrofuran (68.2 mL). The reaction was stirred at −78 Celsius overnight then allowed to warm up to −20 Celsius and stirred at −20 Celsius for 3 h. After quenched with aq. ammonium chloride, the mixture was extracted with ethyl acetate. The combined organic layers were washed with brine, dried and concentrated to dry. The residue was applied on silica gel column, eluting with 0 to 20% EtOAc in hexane, to afford the product (18.1 g, 69.9%). MS (ESI): (M+H)+=456.2. The corresponding diastereoisomer was also obtained (4.52 g, 17.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853243B2
出典データセットuspto-grants-2014_10
ORD IDord-56e1ba27219748ffb40b302fceb35ce9
出典メモuspto-grants-2014_10