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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325178생성일: 2026년 10월 25일

Pyridine → 5,5-Dimethyl-4-(4-(methylsulfonyl)phenyl)-3-(4-methoxyphenyl)-2-(5H)-furanone

https://huagongshe.com/reaction/325178

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물4-Methoxyphenylacetyl chlorideHCID 2734688—
반응물2-Hydroxy-2-methyl-1-(4-(methylsulfonyl)phenyl)propan-1-oneHCID 15428514—
용매Hydrochloric AcidHCID 313—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물5,5-Dimethyl-4-(4-(methylsulfonyl)phenyl)-3-(4-methoxyphenyl)-2-(5H)-furanoneHCID 15516709—

반응 단계

To a cold solution (0° C.) of 2-hydroxy-2-methyl-1-(4-(methylsulfonyl)phenyl)-propane-1-one (726 mg, 3.5 mmol, Step 3), pyridine (0.5 mL, 6.2 mmol) in CH2Cl2 (10 mL) was added 4-methoxyphenylacetyl chloride (1.5 g, 8.4 mmol) over 2 minutes. The resulting yellow solution was stirred at r.t. for 18 h. Then DBU was added in portions every 30 min. (3×1.0 mL, 3×6.7 mmol). The reaction was diluted with EtOAc (100 mL) and 1N HCl (50 mL). The organic layer was washed with water (50 mL), dried over MgSO4 and concentrated. The crude product was purified first by flash chromatography eluted with 40% EtOAc in hexane and then by crystallization in EtOAc and hexane (1:1, 26 mL) to give the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06222048B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-8ff12c79c6c343788b1af6fba6af283c
출처 메모uspto-grants-2001_04