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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395405생성일: 2026년 10월 26일

2,3-Dihydrofuran → Methyl 2-(Difluoromethyl)-4-(2-methylpropyl)-5-[(tetrahydro-2-furyl)thio]-6-(trifluoromethyl)-3-pyridinecarboxylate

https://huagongshe.com/reaction/395405

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DihydrofuranHCID 70934—
반응물Methyl 2-(difluoromethyl)-4-isobutyl-5-mercapto-6-(trifluoromethyl)-3-pyridinecarboxylateHCID 9974711—
촉매2-Methylbenzenesulfonic acidHCID 6925—
용매Diethyl EtherHCID 3283—
생성물Methyl 2-(Difluoromethyl)-4-(2-methylpropyl)-5-[(tetrahydro-2-furyl)thio]-6-(trifluoromethyl)-3-pyridinecarboxylateHCID 2266885968%

반응 단계

A mixture of 7.07 g (0.021 mol) of compound 7, 2.92 g (0.042 mol) of dihydrofuran, and catalytic toluenesulfonic acid (9 mg) in 80 ml of ether was stirred overnight. The reaction mixture was concentrated in vacuo, and the residue was purified by HPLC (20% EtOAc in hexane) to give 5.82 g (68%) of the desired product as a yellow oil, n25D 1.5803.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605624B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-a9da341029bb48f9be78671f29ee9d6a
출처 메모uspto-grants-2003_08