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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1436815생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/1436815

반응식

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 (MgSO4), 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 번호US07618970B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-d4c0be4f1a12448f93016231581be646
출처 메모uspto-grants-2009_11