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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2353360생성일: 2026년 10월 27일

Tetrahydrofuran → [2-(4-Isobutyl-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanol

https://huagongshe.com/reaction/2353360

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물{2-[4-Chloro-3-(trifluoromethyl)phenyl]-1,3-benzoxazol-6-yl}methanolHCID 68453052—
반응물HCID 178448254HCID 178448254—
용매Hydrochloric AcidHCID 313—
생성물[2-(4-Isobutyl-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanolHCID 68453276—

반응 조건

온도100 °C

반응 단계

A mixture of [2-(4-chloro-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanol (1 eq) and Pd(PBut3)2 (0.05 eq) is treated with isobutyl zinc bromide in THF (0.5 M, 3 eq). The resulting mixture is heated at 100° C. in microwave for 30 minutes. The reaction mixture is diluted with aqueous HCl (5%) and extracted with EtOAc. The organic solution is washed with brine and dried over Na2SO4. After concentration, the residue is purified by flash column chromatography (30% EtOAc in hexane) to give the desired intermediate [2-(4-isobutyl-3-trifluoromethyl-phenyl)-benzooxazol-6-yl]-methanol. MS: (ES+): 350.1 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07750021B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-c4438a5e2a234cd480f9e8ee590bbef9
출처 메모uspto-grants-2010_07