돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 229861생성일: 2026년 10월 24일

Sodium Hydroxide → 2-methyl-1-[(S)-1-(tetrahydro-furan-2-yl)methyl]-5-(2-trifluoromethoxy-phenyl)-1H-pyrrole-3-carboxylic acid

https://huagongshe.com/ko/reaction/229861

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물2-methyl-1-[(S)-1-(tetrahydro-furan-2-yl)methyl]-5-(2-trifluoromethoxy-phenyl)-1H-pyrrole-3-carboxylic acid methyl esterHCID 69023243—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매1,4-DioxaneHCID 31275—
생성물2-methyl-1-[(S)-1-(tetrahydro-furan-2-yl)methyl]-5-(2-trifluoromethoxy-phenyl)-1H-pyrrole-3-carboxylic acidHCID 6901998193.5%

반응 단계

To a solution of 171 mg of 2-methyl-1-[(S)-1-(tetrahydro-furan-2-yl)methyl]-5-(2-trifluoromethoxy-phenyl)-1H-pyrrole-3-carboxylic acid methyl ester in dioxane (4 ml) and water (4 ml) was added 1.3 ml of a 1N solution of sodium hydroxide. The reaction mixture was heated at reflux for 20 hours. After such time the reaction mixture was allowed to cool down to room temperature. The mixture was diluted with diethyl ether and extracted with 1N sodium hydroxide solution. Water phases were pooled, acidified with 2N solution of hydrochloride acid and extracted twice with diethyl ether. The organic phases were pooled, washed with brine and dried with MgSO4. Solvent was removed to give 154 mg of the title compound as brownish oil; MS (ISP) 368.0 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07563910B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-5421a429daa2457c8c3e34ed94cd0749
출처 메모uspto-grants-2009_07