반응 #429047
ord-7acf08c544c745649273d04865bc8db7
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후처리
- 1기타The layers were separated
- 2건조the organic layer was dried over sodium sulfate
- 3농축Concentration in vacuo
- 4기타produced a white solid
- 5기타that was triturated from ethyl ether hexanes
- 6여과Filtration
실험 절차
To a solution of 6-methoxybenzo[b]thiophene (18.13 g, 0.111 mol) in 150 mL of anhydrous tetrahydrofuran (THF) at -60° C. was added n-butyllithium (76.2 mL, .122 mol, 1.6 M solution in hexanes), dropwise via syringe. After stirring for 30 minutes, triisopropyl borate (28.2 mL, .122 mol) was introduced via syringe. The resulting mixture was allowed to gradually warm to 0° C. and then distributed between 1N hydrochloric acid and ethyl acetate (300 mL each). The layers were separated, and the organic layer was dried over sodium sulfate. Concentration in vacuo produced a white solid that was triturated from ethyl ether hexanes. Filtration provided 16.4 g (71%) of 6-methoxybenzo[b] thiophene-2-boronic acid as a white solid. mp 200° C. (dec). 1H NMR (DMSC-d6) d 7.83 (s, 1 H) , 7.78 (d, J=8.6 Hz, 1 H) 7.51 (d, J=2.0 Hz, 1 H), 6.97 (dd, J=8.6, 2.0 Hz, 1 H), 3.82 (s, 3 H). FD mass spec: 208.