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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1408730생성일: 2026년 10월 26일

Pyrrolidine → 6-Bromo-3-methyl-2',4',5',6'-tetrahydrospiro[chroman-2,3'-pyran]-4-one

https://huagongshe.com/reaction/1408730

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물2H-Pyran-3(4H)-one, dihydro-HCID 90109—
반응물1-(5-Bromo-2-hydroxyphenyl)propan-1-oneHCID 736409—
용매MethanolHCID 887—
생성물6-Bromo-3-methyl-2',4',5',6'-tetrahydrospiro[chroman-2,3'-pyran]-4-oneHCID 5842402816%

반응 단계

A mixture of 1-(5-bromo-2-hydroxyphenyl)propan-1-one (5.7 g, 25 mol), dihydro-2H-pyran-3(4H)-one (5 g, 50 mmol) and pyrrolidine (3.4 g, 48 mmol) in methanol (80 mL) was stirred overnight. The reaction mixture was removed in vacuo, and H2O was added. The resulting solution was extracted with ethyl acetate. The ethyl acetate solution was dried over anhydrous Na2SO4, filtered, and evaporated to give 6-bromo-3-methyl-2′,4′,5′,6′-tetrahydrospiro[chroman-2,3′-pyran]-4-one (1.2 g, 16%). 1HNMR (CDCl3): 1.16-1.27 (m, 3H), 1.51-1.57 (m, 1H), 1.66-1.73 (m, 1H), 1.91-2.08 (m, 2H), 2.59-2.69 (m, 1H), 3.46-3.56 (m, 2H), 3.88-3.98 (m, 2H), 6.97 (m, 1H), 7.58 (m, 1H), 7.95 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08921359B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-d0e3ba3219f940008f149451505247c9
출처 메모uspto-grants-2014_12