戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1044620作成日:2026年10月27日

1-Iodo-2-methoxyethane → Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate

https://huagongshe.com/reaction/1044620

反応式

関与物質

役割名称HCID仕込み量
反応物1-Iodo-2-methoxyethaneHCID 79136—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物(1R,4S)-methyl 4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylateHCID 10610130—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylateHCID 5983358723%

反応条件

温度-78 °C

反応手順

To a 1.00 M solution of lithium hexamethyldisilazide in tetrahydrofuran (9.1 mL, 9.1 mmol) under N2 at −78° C. was added a solution of methyl (1R,4S)-4-[(tert-butoxycarbonyl)amino]cyclopent-2-ene-1-carboxylate (1.0 g, 4.1 mmol) in tetrahydrofuran (2.0 mL). The resulted light brown solution was stirred at −78° C. for 30 min before adding a solution of 1-iodo-2-methoxyethane (0.93 g, 5.0 mmol) in tetrahydrofuran (2.0 mL). The mixture was stirred for an hour at −78° C. then kept in a freezer reading at −20° C. overnight. The reaction was quenched with saturated ammonium chloride. The layers were separated and the aqueous extracted with ether three times. The combined organics were then washed with brine, dried (MgSO4), filtered and purified by flash chromatography (EtOAc/Hexane) to provide the desired product (0.28 g, 23%). LCMS calculated for C5H26NO5: (M+H) 300.2; found 300.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08563582B2
出典データセットuspto-grants-2013_10
ORD IDord-8cabd21508a74df0a61e286dd16ac49a
出典メモuspto-grants-2013_10