Trimethyl borate → 3,3-bis(fluoromethyl)-5-methylbenzo[c][1,2]oxaborol-1(3H)-ol
반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[C:9]([O:14]COCC)([CH2:12][F:13])[CH2:10][F:11].[Li]CCCC.[B:24](OC)(OC)[O:25]C.CC(=O)OCC>C1COCC1>[F:11][CH2:10][C:9]1([CH2:12][F:13])[O:14][B:24]([OH:25])[C:2]2[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]1=2참가 물질
6
실험 절차
To a solution of 1-bromo-2-(2-(ethoxymethoxy)-1,3-difluoropropan-2-yl)-4-methylbenzene (1.8 g, 5.10 mmol) in THF (15 mL) at −78° C. was slowly added n-BuLi (5.1 mL, 12.75 mmol). After stirring for 10 min, a solution of B(OMe)3 (1.06 g, 10.2 mmol) in dry THF (5 mL) was added dropwise. The mixture was stirred at −78° C. for 0.5 h, and then dry ice bath was removed. The solution was acidified with HCl (4 N) and extracted with EA (100 mL×2). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE:EA (5:1 to 3:1) to give the desired compound (350 mg, yield 32%) as white solid.
후처리
- customat −78° C.
- stirringThe mixture was stirred at −78° C. for 0.5 h
- customdry ice bath was removed
- extractionextracted with EA (100 mL×2)
- washThe combined organic layers were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by column chromatography over silica gel
- washeluted with PE
출처 및 근거
- ORD 기록
- ord-83816ec589a74581bcdd58fd995b6284
- 출처 데이터셋
- uspto-grants-2014_10
- 특허 번호
- US08853186B2
반응 노트
불러오는 중…