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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 반응물 | (1R,4S)-methyl 4-(tert-butoxycarbonylamino)cyclopent-2-enecarboxylate | HCID 10610130 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Methyl(1S,4S)-4-[(tert-Butoxycarbonyl)amino]-1-(2-methoxyethyl)cyclopent-2-ene-1-carboxylate | HCID 59833587 | 23% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07618970B2 |
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| 출처 데이터셋 | uspto-grants-2009_11 |
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| ORD ID | ord-d4c0be4f1a12448f93016231581be646 |
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| 출처 메모 | uspto-grants-2009_11 |
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