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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 736807생성일: 2026년 10월 24일

Methyl cyclopent-1-ene-1-carboxylate → HCID 86607904, 화합물

https://huagongshe.com/ko/reaction/736807

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참여 물질

역할이름HCID투입량
반응물Methyl cyclopent-1-ene-1-carboxylateHCID 549129—
반응물(+)-BenzylphenethylamineHCID 1268086—
반응물(1R,8R)-11,11-dimethyl-5-oxa-3lambda6-thia-4-azatetracyclo[6.2.1.01,6.04,6]undecane 3,3-dioxideHCID 16212283—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 86607904HCID 86607904—

반응 조건

온도-78 °C

반응 단계

According to the procedure of Tet. Asymm., 13, 2002, 1555: To a solution of (R)-N-benzyl-N-α-methylbenzylamine (1.37 mL, 2 eq.) in THF (10 mL) at −78° C. was added n-butyllithium (2.4 M, 2.2 mL, 1.6 eq). The reaction was allowed to stir for 30 min at −78° C. and then methyl 1-cyclopentene-1-carboxylate (0.41 mL, 3.25 mmol, 1 eq) was added dropwise. The reaction was stirred for 3 h at −78° C. and then a solution of (1R)-(−)-(10-camphorsulfonyl)oxaziridine (1.49 g, 2 eq) in THF (12 mL) was added dropwise via cannula. The reaction was allowed to stir at room temperature overnight, and was then taken up in ethyl acetate, washed with NaHCO3 (1×), brine (2×), dried over Na2SO4, filtered and concentrated. Purification by silica chromatography eluting with a gradient of 10-15% ethyl acetate/hexanes afforded methyl (1R,2R)-2-{benzyl[(1R)-1-phenylethyl]amino}-1-hydroxycyclopentanecarboxylate as an off white solid (0.77 g, 69%). MS: 354.2 (M+H)+

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07595327B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-6692c222604a422190905e5c5ec97def
출처 메모uspto-grants-2009_09