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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1527979생성일: 2026년 10월 26일

2-Ethyl-2-methyl-1,3-dioxolane → (R)-6-(2-(2-(4-Bromophenyl)-2-o-tolylethyl)-1,3-dioxolan-2-yl)-2-methylpyridazin-3(2H)-one

https://huagongshe.com/reaction/1527979

반응식

참여 물질

역할이름HCID투입량
반응물2-Ethyl-2-methyl-1,3-dioxolaneHCID 61067—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물HCID 86684807HCID 86684807—
생성물(R)-6-(2-(2-(4-Bromophenyl)-2-o-tolylethyl)-1,3-dioxolan-2-yl)-2-methylpyridazin-3(2H)-oneHCID 8668481016.2%

반응 단계

A solution of (R)-6-(3-(4-bromophenyl)-3-o-tolylpropanoyl)-2-methylpyridazin-3(2H)-one (example 8, step 3; 235 mg, 571 μmol), and p-toluenesulfonic acid monohydrate (10.9 mg, 57.1 μmol) in 2-ethyl-2-methyl-1,3-dioxolane (2.33 g, 20.0 mmol) was heated for 45 min at 110° C., then partitioned between sat. aq. sodium hydrogencarbonate solution and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, filtered, and evaporated. Chromatography (SiO2; gradient heptane-ethyl acetate) produced the title compound (42 mg, 16%). White semisolid, MS: 455.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09090565B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-f25f85b7f8734bd285844912a2c23187
출처 메모uspto-grants-2015_07