돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76770생성일: 2026년 10월 24일

3,5-Dinitrobenzoic acid → 3,5-Dinitrobenzyl alcohol

https://huagongshe.com/ko/reaction/76770

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dinitrobenzoic acidHCID 7433—
반응물Boron trifluoride etherateHCID 8000—
반응물Sodium borohydrideHCID 4311764—
용매TetrahydrofuranHCID 8028—
생성물3,5-Dinitrobenzyl alcoholHCID 11697867.1%

반응 조건

온도25 °C

반응 단계

To a suspension of NaBH4 (2.85 g, 75.4 mmol) in dry THF (40 mL) at 0° C. was added a solution of 3,5-dinitrobenzoic acid (8.0 g, 37.7 mmol) in THF (20 mL), followed by the addition of BF3.OEt2 (12.5 mL, 98.0 mmol). The resulting mixture was warmed to 25° C. and stirred for 1 hour after which the reaction was quenched with 1 M HCl. The aqueous phase was extracted with DCM and the organic phase was then washed with saturated Na2CO3. The organic phase was dried over MgSO4 and evaporated under reduced pressure to give the title compound 6 as an orange solid (5.01 g, 25.3 mmol, 67%). 1H NMR (400 MHz, ((CD3)2C)) δ 8.91 (t, J=0.4 Hz, 1H), 8.57 (dd, J=1.2, 2.0 Hz, 2H), 4.93 (d, J=5.2 Hz, 2H), 3.57 (bs, 1H); 13C NMR (75 MHz, (CD3)2CO) δ 149.4, 148.4 (2C), 127.0 (2C), 117.6, 62.8; HRMS (ESI) Calculated for C7H5N2O5 [M−H]−: 197.0204. Found: 197.0200. m.p.: 89° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835641B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-e112f3baabb245bab835d1a01f723b9f
출처 메모uspto-grants-2014_09