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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1752810생성일: 2026년 10월 25일

Methyl 4-(p-chlorophenoxy)butyrate → HCID 178508402, 화합물

https://huagongshe.com/reaction/1752810

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 4-(p-chlorophenoxy)butyrateHCID 547990—
반응물HCID 178513185HCID 178513185—
용매PyridineHCID 1049—
생성물HCID 178508402HCID 17850840272.3%

반응 조건

온도125 °C

반응 단계

A mixture of methyl 4-(4-chlorophenoxy)butanoate (1.4 g, 6.13 mmol), aminoguanidine bicarbonate (2.08 g, 15.3 mmol), and pyridine (12 mL) was added to a 100 mL RBF with a magnetic stirring bar. The flask was fitted with a condenser, and heated to 125° C. using an oil bath. Progress of the reaction was monitored by analytical HPLC with UV detection at 215 nm. The mixture was heated for 20 hours, and an additional portion of aminoguanidine bicarbonate (0.60 g, 4.4 mmol) was added. After an additional 22 hours of heating, the reaction was complete. The reaction allowed to cool to ambient temperature, concentrated under reduced pressure and partitioned between ethyl acetate (50 mL) and water (20 mL). The aqueous layer was extracted once more with ethyl acetate (30 mL). The combined organic layers were washed with saturated aqueous NaCl (2×15 mL), dried (Na2SO4), filtered and concentrated. Dichloromethane (5 mL) was added and a precipitate that formed was isolated by filtration, rinsed with dichloromethane (5 mL), and then dried under reduced pressure to afford the title compound as a white powder (1.12 g, 72% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09163027B2
출처 데이터셋uspto-grants-2015_10
ORD IDord-0a2a1c94b35f4b6983e27be13a24dc43
출처 메모uspto-grants-2015_10