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HRID 1752810作成日:2026年10月24日

Methyl 4-(p-chlorophenoxy)butyrate → HCID 178508402、化合物

https://huagongshe.com/ja/reaction/1752810

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-(p-chlorophenoxy)butyrateHCID 547990—
反応物HCID 178513185HCID 178513185—
溶媒PyridineHCID 1049—
生成物HCID 178508402HCID 17850840272.3%

反応条件

温度125 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09163027B2
出典データセットuspto-grants-2015_10
ORD IDord-0a2a1c94b35f4b6983e27be13a24dc43
出典メモuspto-grants-2015_10