364-12-5, The chemical industry reduces the impact on the environment during synthesis 364-12-5, name is 5-Bromo-2-iodobenzotrifluoride, I believe this compound will play a more active role in future production and life.
(1) Synthesis of 1-[4-bromo-2-(trifluoromethyl)phenyl]cyclobutanol To a solution of 5-bromo-2-iodobenzotrifluoride (5.00 g) in dehydrated tetrahydrofuran (140 mL), n-butyl lithium (2.69 mol/L, solution in n-hexane, 5.30 mL) was added at -78C and the mixture was stirred at that temperature for 25 minutes. After adding a solution of cyclobutanone (999 mg) in tetrahydrofuran (5.00 mL), the mixture was brought to room temperature and stirred for 3 days. After adding a saturated aqueous solution of ammonium chloride under cooling with ice, two extractions were conducted with ethyl acetate. The combined organic layers were washed with water and thereafter dried over anhydrous magnesium sulfate. After removing the desiccant by filtration, the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate = 98:2-80:20) to give 1-[4-bromo-2-(trifluoromethyl)phenyl]cyclobutanol as a pale yellow oil (3.00 g). 1H NMR (300 MHz, CHLOROFORM-d) delta ppm 1.71 – 1.88 (m, 1 H) 2.20 – 2.49 (m, 3 H) 2.52 – 2.70 (m, 2 H) 7.29 – 7.35 (m, 1 H) 7.62 – 7.69 (m, 1 H) 7.78 – 7.84 (m, 1 H). MS EI posi: 294[M]+.
The chemical industry reduces the impact on the environment during synthesis 5-Bromo-2-iodobenzotrifluoride. I believe this compound will play a more active role in future production and life.
Reference:
Patent; Taisho Pharmaceutical Co., Ltd.; TAKAYAMA, Tetsuo; SHIBATA, Tsuyoshi; SHIOZAWA, Fumiyasu; KAWABE, Kenichi; SHIMIZU, Yuki; HAMADA, Makoto; HIRATATE, Akira; TAKAHASHI, Masato; USHIYAMA, Fumihito; OI, Takahiro; SHIRASAKI, Yoshihisa; MATSUDA, Daisuke; KOIZUMI, Chie; KATO, Sota; EP2881384; (2015); A1;,
Iodide – Wikipedia,
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