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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 510599생성일: 2026년 10월 26일

Ethyl Acetate → 7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromene-4-carboxylic acid

https://huagongshe.com/reaction/510599

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Trimethylsilyl cyanideHCID 82115—
반응물7-fluoro-2,2-dimethyl-3,4-dihydro-2H-1-benzopyran-4-oneHCID 15205373—
촉매zinc(II)iodideHCID 9883512—
용매Hydrochloric AcidHCID 313—
생성물7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromene-4-carboxylic acidHCID 6708039424.25%

반응 조건

온도50 °C

반응 단계

To 7-fluoro-2,2-dimethyl-2,3-dihydrochromen-4-one (1.000 g, 5.149 mmol) was added trimethylsilyl cyanide (3.215 mL, 25.75 mmol) followed by a spatula tip of zinc iodide. The reaction was heated at 50° C. for 1 hour. The reaction was cooled, diluted with ethyl acetate (40 mL) and washed with saturated sodium bicarbonate (2×25 mL), brine (25 mL), dried over magnesium sulfate and concentrated. The product was dissolved in 5 mL of acetic acid and 5 mL of HCl, and SnCl2 dihydrate (4.648 g, 20.60 mmol) was added. The reaction heated at reflux (130° C. oil bath temperature) overnight. The reaction was cooled, diluted with ethyl acetate (50 mL), washed with water (50 mL) and brine (50 mL), dried over magnesium sulfate and concentrated. The residue was purified by silica gel chromatography over silica gel eluting with a gradient of 0.5% MeOH/CH2Cl2 containing 0.5% acetic acid to 10% MeOH/CH2Cl2 containing 0.5% acetic acid to provide the title compound (0.280 g, 24.25% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096567B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-b2ae9b44d71843cfa771a960258185cf
출처 메모uspto-grants-2015_08