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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 376343생성일: 2026년 10월 25일

Triethylamine → 5-Hydroxy-4-(4-methanesulfonyl-phenyl)-5-methyl-3-phenylsulfanyl-5H-furan-2-one

https://huagongshe.com/reaction/376343

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(Phenylthio)acetic acidHCID 59541—
반응물Carbonyl bromideHCID 79057—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2-Bromo-1-[4-(methanesulfonyl)phenyl]propan-1-oneHCID 13207839—
용매AcetonitrileHCID 6342—
생성물5-Hydroxy-4-(4-methanesulfonyl-phenyl)-5-methyl-3-phenylsulfanyl-5H-furan-2-oneHCID 15461522—

반응 단계

To a mixture of 2-bromo-1-(4-(methylsulfonyl)phenyl) propan-1-one (6.0 g, 20.6 mmol) and thiophenoxyacetic acid (3.8 g, 22.6 mmol) in acetonitrile (60 mL) was added triethylamine (4.0 mL, 28.8 mmol). The mixture was stirred at r.t. for 3 h. T.L.C. showed no bromoketone remaining and DBU (4.0 mL) was added. The mixture was stirred at r.t. for 1 h., then air was bubbled through the mixture for another hour. After dilution with water, the mixture was extracted with EtOAc. The EtOAc extract was washed with 1N aqueous HCl, brine, dried over MgSO4, filtered and the solvent evaporated under vacuum. The residue was swished in Et2O to give the title compound (6.0 g as a pale yellow powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06020343
출처 데이터셋uspto-grants-2000_02
ORD IDord-6995c775a8d24ed3ad37503f6175cb95
출처 메모uspto-grants-2000_02