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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 453843생성일: 2026년 10월 25일

Hydrochloric Acid → 1-(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-pyrrolidine-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/453843

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물MethanolHCID 887—
반응물BoronHCID 5462311—
반응물1-(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl esterHCID 66727299—
용매TetrahydrofuranHCID 8028—
생성물1-(2,3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-pyrrolidine-3-carboxylic acid methyl esterHCID 66727025—

반응 조건

온도0 °C

반응 단계

A solution containing 300 mg (1.03 mmol) of 1-(2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-5-oxo-pyrrolidine-3-carboxylic acid methyl ester in dry tetrahydrofuran (4 mL) was cooled to 0° C. under nitrogen. After adding 4 mL of 1M BH3-tetrahydrofuran solution (4.12 mmol), the reaction mixture was allowed to warm to room temperature and it was stirred for 5 h. Decomposition of the boron complexes was effected by addition of 3 mL of methanol and 3 mL of 6 M HCl-solution followed by stirring the mixture at 40° C. for ½ h. Tetrahydrofuran was evaporated off under vacuum. The residue was dissolved in 50 mL of water and the pH of the solution was adjusted to 10 using 1M Na2CO3 solution. The water phase was extracted with ethyl acetate (3×25 mL), and the combined organic phases were dried over anhydrous sodium sulfate, filtered, and evaporated to dryness. The crude product was purified by column chromatography (silica gel, heptane/ethyl acetate, 7:3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08492549B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-18652c8fe31344f5b052a735010d2a7e
출처 메모uspto-grants-2013_07