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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1466736생성일: 2026년 10월 27일

Methanesulfonic Acid → Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonate

https://huagongshe.com/reaction/1466736

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물Phthalaldehydic acidHCID 8406—
반응물Dimethyl ester phosphorous acidHCID 94853—
반응물SodiumHCID 5360545—
용매MethanolHCID 887—
생성물Dimethyl (3-oxo-1,3-dihydro-2-benzofuran-1-yl)phosphonateHCID 1111821367.3%

반응 단계

To dry methanol (40 ml) was slowly added sodium (1.15 g, 50 mmol) at 0 under N2 atmosphere while stirring, then added dimethyl hydrogen phosphite (5.5 g, 50 mmol), and 2-formylbenzoic acid (5.25 g, 35 mmol). The ice bath was removed and the reaction mixture was stirred for 30 min at room temperature, and then the reaction mixture was slowly added methanesulfonic acid (5.5 g, 55 mmol) and concentrated at reduced pressure to give the crude residue. The crude residue was partitioned between DCM and cold water (100 ml each), and the organic phase was washed with water and brine, dried over sodium sulphate, filtered, and concentrated to give the crude product (5.7 g, 67%) as an off white solid, used in next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08999985B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-a3ab18e4471645d0a8bbf30424b95826
출처 메모uspto-grants-2015_04