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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 325191생성일: 2026년 10월 24일

Formaldehyde → 5-Hydroxymethyl-4-(4-(methylsulfonyl)phenyl)-3-phenyl-2-(5H)-furanone

https://huagongshe.com/ko/reaction/325191

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물RofecoxibHCID 5090—
반응물TetrahydrofuranHCID 8028—
반응물Potassium CarbonateHCID 11430—
용매WaterHCID 962—
생성물5-Hydroxymethyl-4-(4-(methylsulfonyl)phenyl)-3-phenyl-2-(5H)-furanoneHCID 22002636—
생성물5,5-bis(hydroxymethyl)-3-phenyl-4-(4-(methylsulfonyl)phenyl)-2-(5H)-furanoneHCID 22002653—

반응 단계

A mixture of 3-phenyl-4-(4-(methylsulfonyl)phenyl)-2-(5H)-furanone from Step 1 (0.31 g, 1.0 mmol), 37% aqueous formaldehyde solution (0.1 mL), THF (20 mL) and water (5 mL) was treated with K2CO3 (20 mg, 0.15 mmol). After stirring for 1 h at room temperature, the reaction mixture was quenched with 15 mL of saturated aqueous NH4Cl and extracted with 50 mL of EtOAc. The extract was dried over MgSO4 and concentrated. The residue was purified by flash chromatography eluting with 3:1 EtOAc/hexanes to give 50 mg of the title compound along with 120 mg of 5,5-bis(hydroxymethyl)-3-phenyl-4-(4-(methylsulfonyl)phenyl)-2-(5H)-furanone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06222048B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-c5a18eb3f1f343afb394a3a348a0ce3f
출처 메모uspto-grants-2001_04