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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349348생성일: 2026년 10월 24일

Sodium hydride → HCID 69020248, 화합물

https://huagongshe.com/ko/reaction/349348

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Dimethyl [3-(3-chlorophenyl)-2-oxopropyl]phosphonateHCID 12989750—
반응물[4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl esterHCID 86595299—
용매TetrahydrofuranHCID 8028—
생성물HCID 69020248HCID 6902024834%

반응 단계

Sodium hydride (60% dispersion in oil, 35 mg, 0.88 mmol) was added to a solution of [3-(3-chlorophenyl)-2-oxopropyl]-phosphonic acid dimethyl ester (221 mg, 0.80 mmol) in THF (2.0 mL) at 0° C. After 1 h at 0° C., [4-((R)-2-formyl-6-oxo-piperidin-1-yl)-butoxy]-acetic acid ethyl ester (0.88 mmol, crude) in THF (2 mL) was added via cannula. The reaction was allowed to warm to rt. After 18 h at rt, the reaction was quenched with aqueous acetic acid (50%, 10 mL) and extracted with EtOAc (3×20 mL). The combined organic phase was washed with brine (25 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (20% →40% EtOAc/CH2Cl2, gradient) afforded 117 mg (34%) of (4-{(R)-2-[(E)-4-(3-chlorophenyl)-3-oxo-but-1-enyl]-6-oxo-piperidin-1-yl}-butoxy)-acetic acid ethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179820B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-0d6484f6104048d9a4bc30d491aac73c
출처 메모uspto-grants-2007_02