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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20922생성일: 2026년 10월 24일

Pyridine → 3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-pyrrolidine-1-carboxylic Acid Benzyl Ester

https://huagongshe.com/ko/reaction/20922

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-DimethylaminopyridineHCID 21885—
반응물1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
반응물3-Hydroxy-4-hydroxymethyl-pyrrolidine-1-carboxylic Acid Benzyl EsterHCID 23062049—
생성물3-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-pyrrolidine-1-carboxylic Acid Benzyl EsterHCID 131728223—

반응 단계

Referring to scheme 18, compound 74 (4.39 g, 17.5 mmol) was co-evaporated with anhydrous pyridine three times and then dissolved in pyridine (30 mL). To this solution dimethylamino pyridine (0.213 g, 1.75 mmol) and DMT-Cl (6.22 g, 18.4 mmol, 1.05 equiv.) were added at room temperature. The reaction mixture was stirred at room temperature for 16 h. The excess DMT-Cl was quenched by the addition of methanol (10 mL). The solution was dried under reduced pressure. To the residue was suspended in ethyl acetate (300 mL) and washed with saturated bicarbonate solution, brine and water. The organic layer was dried over anhydrous sodium sulfate, filtered and evaporated. The crude product was obtained after removal of the solvent. Upon purification over silica gel using 3% MeOH/DCM compound 75 (8.46 g, 87%) was obtained as white foamy solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745608B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-32593fb04bdc44d59d30b88895bd07e6
출처 메모uspto-grants-2010_06