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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2056738생성일: 2026년 10월 26일

Trifluoroacetic acid → 6-bromo-1H,3H-naphtho[1,8-cd]pyran

https://huagongshe.com/reaction/2056738

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물TriethylsilaneHCID 12052—
반응물1H,3H-Naphtho(1,8-cd)pyran-1,3-dione, 6-bromo-HCID 66493—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물6-bromo-1H,3H-naphtho[1,8-cd]pyranHCID 69307283—

반응 단계

To 6-bromo-1H,3H-naphtho[1,8-cd]pyran-1,3-dione (1.5 g, 5.4 mmol) in ethanol (10 mL) was added sodium borohydride (0.41 g, 10.8 mmol) and the mixture stirred at room temperature for 1 h. The reaction was quenched with 3M hydrochloric acid and extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. The residue was dissolved in dichloromethane and trifluoroacetic acid (1.05 mL, 13.53 mmol) and triethylsilane (4.3 mL, 27 mmol) added. After stirring for 5 min at room temperature, the solvent was removed in vacuo and the residue purified by column chromatography on silica gel, eluting with dichloromethane, to yield 6-bromo-1H,3H-naphtho[1,8-cd]pyran as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07335660B2
출처 데이터셋uspto-grants-2008_02
ORD IDord-93f7594914514440b42af07036f86d83
출처 메모uspto-grants-2008_02