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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 277785생성일: 2026년 10월 25일

(2R)-Oxiran-2-ylmethyl butanoate → HCID 54330421, 화합물

https://huagongshe.com/reaction/277785

반응식

참여 물질

역할이름HCID투입량
반응물(2R)-Oxiran-2-ylmethyl butanoateHCID 2724536—
반응물3,6-Dihydro-4-[4-[[(phenylmethoxy)carbonyl]amino]phenyl]-1(2H)-pyridinecarboxylic acid phenylmethyl esterHCID 54271798—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물HCID 54330421HCID 54330421—

반응 조건

온도-78 °C

반응 단계

A solution of 3,6-dihydro-4-[4-[[(phenylmethoxy)carbonyl]amino]phenyl]-1(2H)-pyridinecarboxylic acid phenylmethyl ester (EXAMPLE 17, Step 2, 0.500 g) in dry tetrahydrofuran (5.7 mL) at −78° C. under N2 is treated with n-butyllithium (0.73 mL, 1.6M in hexanes) dropwise over five minutes. The resulting mixture is stirred at −78° C. for 45 minutes and is then treated with (R)-(−)-glycidyl butyrate dropwise. The resulting solution is allowed to warm to ambient temperature over approximately 45 minutes and is stirred for an additional 20 hours, after which the reaction is quenched with saturated aqueous ammonium chloride (10 mL), diluted with water (20 mL) and extracted with ethyl acetate (2×15 mL). The combined organic phase is washed with saline (10 mL), dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the crude product which is chromatographed on silica gel (230-400 mesh, 40 g), eluting with methanol/methylene chloride (1/99). Pooling and concentration of those fractions with an Rf=0.37 by TLC (methanol/chloroform, 5/95) gives the title compound, mp 131.5-133.5° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358942B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-42ee1b32a40943088d2cca5fa55b4207
출처 메모uspto-grants-2002_03