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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41133생성일: 2026년 10월 24일

Imidazole → HCID 59027527, 화합물

https://huagongshe.com/ko/reaction/41133

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물FlamenolHCID 71648—
반응물tert-ButyldiphenylchlorosilaneHCID 94078—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물HCID 59027527HCID 5902752733%

반응 단계

tert-Butyldiphenylsilylchloride (TBDPSCl) (1.8 mL, 1.96 g, 7.14 mmol) was added to a suspension of 5-methoxyresorcinol 18 (1.0 g, 7.14 mmol) and imidazole (729 mg, 10.71 mmol) in dry DMF (5 mL) under argon at −22° C. and the mixture was stirred for 10 min. The reaction mixture was diluted with H2O (25 mL) and extracted with EtOAc (3×25 mL). The combined organic extracts were washed with aq 1M of HCl (2×25 mL), and brine (2×25 mL). The organic layer was then dried (Na2SO4) and concentrated in vacuo. The crude silyl phenol 19 was purified by FCC on silica gel (5% ethyl acetate in hexane) to afford pure silyl phenol 19 (892 mg, 33%): 1H NMR (300 MHz, CDCl3) δ 7.89-7.75 (4H, m, HAr), 7.48-7.34 (6H, m, HAr), 5.98 (2H, t, J=2.1 Hz, HAr), 5.92 (1H, t, J=2.1 Hz, HAr), 5.13 (1H, br, s, HO—), 3.56 (3H, s, H3CO), 1.14 (9H, s, [(H3C)3C]; 13C NMR (75 MHz, CDCl3) δ 161.1, 157.3, 156.8, 135.4, 132.8, 129.9, 127.7, 100.1, 98.5, 95.0, 55.0, 26.4, 19.4; LRMS (CI), m/z (relative intensity): 378([M+1]+, 30), 321 (100), 243 (30), 213 (10), 199 (29). This material was employed directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530512B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-69ea5fcdb2f84d7c8f92d66bcf1f07b7
출처 메모uspto-grants-2013_09