돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 565101생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/565101

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 1 N aquous 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 번호US06169188A
출처 데이터셋uspto-grants-2001_01
ORD IDord-03a5acb0820a48dd9035e26defb5b0a9
출처 메모uspto-grants-2001_01