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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1680827생성일: 2026년 10월 26일

Benzyl Bromide → Benzyl 6,6-dibromopenicillanate

https://huagongshe.com/reaction/1680827

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl BromideHCID 7498—
반응물TriethylamineHCID 8471—
반응물6,6-Dibromopenicillanic acidHCID 90376—
용매DimethylacetamideHCID 31374—
생성물Benzyl 6,6-dibromopenicillanateHCID 1093928595%

반응 단계

To a solution of 54 g. (0.165 mole) of 6,6-dibromopenicillanic acid in 350 ml. of N,N-dimethylacetamide was added 22.9 ml. (0.165 mole) of triethylamine and the solution was stirred for 40 minutes. Benzyl bromide (19.6 ml., 0.165 mole) was added and the resulting mixture was stirred at room temperature for 48 hours. The precipitated triethylamine hydrobromide was filtered off, and the filtrate was added to 1,500 ml. of ice-water, adjusted to pH 2. The mixture was extracted with ether, and the extracts were washed successively with saturated sodium bicarbonate, water and brine. The dried (MgSO4) ether solution was evaporated in vacuo to give an off-white solid, which was recrystallized from isopropanol. This afforded 70.0 g. (95% yield) of the title compound m.p. 75°-76° C. The IR spectrum (KBr disc) showed absorptions at 1795 and 1740 cm-1. The NMR spectrum (CDCl3) showed absorptions at 1.53 (s, 3H), 1.58 (s, 3H), 4.50 (s, 1H), 5.13 (s, 2H), 5.72 (s, 1H) and 7.37 (s, 5H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04276285
출처 데이터셋uspto-grants-1981_06
ORD IDord-52fda15eda2a445e83622c34bf6e954b
출처 메모uspto-grants-1981_06