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HRID 72391作成日:2026年10月25日

Triethylamine → (S)-Methyl 4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoate

https://huagongshe.com/reaction/72391

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物(S)-tert-Butyl (1-(4-bromophenyl)ethyl)carbamateHCID 56973617—
触媒palladium(II) acetateHCID 167845—
溶媒Diethyl EtherHCID 3283—
溶媒N,N-dimethylformamide methanolHCID 21901440—
生成物(S)-Methyl 4-(1-((tert-butoxycarbonyl)amino)ethyl)benzoateHCID 57432297176.2%

反応条件

温度80 °C

反応手順

A mixture of (S)-tert-butyl (1-(4-bromophenyl)ethyl)carbamate (D1) (9.20 g, 27.3 mmol), 1,3-bis(diphenylphosphino)-propane (2.25 g, 5.46 mmol), palladium (II) acetate (1.22 g, 5.46 mmol), and triethylamine (11.5 ml, 81.9 mmol) in N,N-dimethylformamide/methanol (60 ml/60 ml) was stirred at 80° C. overnight under carbon monoxide atmosphere. After cooling to room temperature, the mixture was diluted with ether (300 ml) and washed with water (3×100 ml). The organic layer was dried over Na2SO4 and evaporated in vacuo. The residue was purified by flash chromatography on silica gel eluting with a mixture petroleum ether/ethyl acetate 5:1 to afford the title compound (D2) (6.72 g) as white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08828987B2
出典データセットuspto-grants-2014_09
ORD IDord-b5675bee7ce140d7acfffb54da8569a9
出典メモuspto-grants-2014_09