돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 643427생성일: 2026년 10월 26일

Hydrochloric Acid → 7-(Trifluoromethyl)-1H-indole

https://huagongshe.com/reaction/643427

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Boron trifluoride etherateHCID 8000—
반응물7-TrifluoromethylisatinHCID 604575—
반응물Sodium borohydrideHCID 4311764—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물7-(Trifluoromethyl)-1H-indoleHCID 10419882—

반응 조건

온도-20 °C

반응 단계

To a stirred mixture of 7-trifluoromethyl-1H-indole-2,3-dione (116 mg) in THF (5.00 mL) was added boron trifluoride etherate (0.205 mL, 1.62 mmol) followed by sodium borohydride (71.4 mg, 1.88 mmol). The resulting mixture was stirred at −20° C. for 2 hrs, then water (1 mL) was added and the mixture was stirred at 0° C. for 10 min. The solution was acidified to pH=1 with 2N HCl, warmed to r.t. and stirred at r.t. for 20 min prior to extraction with EtOAC. The extracts were dried over magnesium sulphate, concentrated in vacuo and the residue purified by chromatography over silica gel eluting with hexane to give 7-trifluoromethyl-1H-indole. 1H NMR (400 MHz, CDCl3) δ ppm 6.63-6.68 (1H, m), 7.20 (1H, t, J=7.71 Hz), 7.30-7.35 (1H, m), 7.47 (1H, d, J=7.33 Hz), 7.83 (1H, d, J=8.08 Hz), and 8.56 (1H, br. s.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07700594B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-b180d9a9da1444b0acb1354b7df3bf96
출처 메모uspto-grants-2010_04