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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270603생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/270603

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참여 물질

역할이름HCID투입량
반응물1-Iodo-2-methoxyethaneHCID 79136—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물(1R,4S)-methyl 4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylateHCID 10610130—
용매TetrahydrofuranHCID 8028—
생성물Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylateHCID 5983358723%

반응 조건

온도-78 °C

반응 단계

To a 1.00 M solution of lithium hexamethyldisilazide in tetrahydrofuran (9.1 mL, 9.1 mmmol) 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 (magnesium sulfate), filtered and purified by flash chromatography (EtOAc/Hexane) to provide the desired product (0.28 g, 23%). LCMS calculated for C15H26NO5: (M+H) 300.2; found 300.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449467B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-60d4d87c1df4495cab843cd4e6456894
출처 메모uspto-grants-2008_11