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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1263079생성일: 2026년 10월 27일

Diethyl Ether → Octane, 1-bromo-8-fluoro-

https://huagongshe.com/reaction/1263079

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물(Diethylamino)sulfur trifluorideHCID 123472—
반응물1-Octanol, 8-bromo-HCID 162607—
반응물Sodium BicarbonateHCID 516892—
용매DichloromethaneHCID 6344—
생성물Octane, 1-bromo-8-fluoro-HCID 1162561.3%

반응 조건

온도-78 °C

반응 단계

A solution of 8-bromooctan-1-ol (Hendry et al., J. Chem. Ecol., 1, 317, 1975), (2.50 g, 11.9 mmol) in methylene chloride (about 3 ml) is slowly added to a stirred solution of diethylaminosulfur trifluoride (DAST) (Middleton, J. Org. Chem, 40, 574, 1975) (1.5 mL, 11.9 mmol) in methylene chloride (10 mL), cooled to -78° C. After the addition is completed, the reaction mixture is warmed to 25° C. and saturated aqueous sodium bicarbonate (about 5 mL) is added, followed by dilution with ether (about 200 mL). The organic layer is then separated, and washed with water (20 mL), saturated sodium bicarbonate (20 mL) and then dried (MgSO4). The volatiles are removed in vacuo and the crude product is purified by flash chromatography using hexane/ethyl acetate, (95.5, v/v) to afford 8-bromo-fluoro-octane (1.54 g, 61%) as a clear colorless liquid: Rf=0.70, hexane/ethyl acetate (7:3, v/v); IR (film) ν2850-3000 (alkane CH) and 1H-NMR (CDCl3) δ1.15-2.0 (m, 12H), 3.39 (t, J=6 Hz, 2H), 4.42 (dt, J=48 Hz, 6 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04455441
출처 데이터셋uspto-grants-1984_06
ORD IDord-75032fc405b949d29e2ca1f049d83155
출처 메모uspto-grants-1984_06