反応式
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[F:8].C([Li])CCC.C([O:17][B:18](OC(C)C)[O:19]C(C)C)(C)C.Cl>O1CCCC1>[F:1][C:2]1[C:3]([F:8])=[CH:4][CH:5]=[CH:6][C:7]=1[B:18]([OH:19])[OH:17]参加物
反応条件
- 温度
- -70 °C
実験手順
After 7.5 g of o-difluorobenzene was dissolved in 80 ml of dried tetrahydrofuran (THF), the solution thus formed was cooled down to -70° C. under a nitrogen atmosphere and then added dropwise with 42 ml of butyllithium (1.6 mol/liter hexane solution) at a temperature lower than -55° C. The solution was continuously stirred at the same temperature for 1.5 hours and added dropwise with a THF solution containing 24.8 g of triisopropylborate at a temperature of -65° C. to -60° C. After the dropping of the solution was finished, the solution was continuously stirred at an ambient temperature for 12 hours, added further with 60 ml of a 10% aqueous hydrochloric acid solution, and continuously stirred for 1 hour. The reaction mixture thus obtained was subjected to extraction with an ether, washed with water, dried, and subjected to distillation under a reduced pressure to separate the solvent to obtain 9.0 g of 2,3-difluorophenyl boronic acid.
後処理
- customthe solution thus formed
- stirringthe solution was continuously stirred at an ambient temperature for 12 hours
- stirringcontinuously stirred for 1 hour
- customThe reaction mixture thus obtained
- extractionwas subjected to extraction with an ether
- washwashed with water
- customdried
- distillationsubjected to distillation under a reduced pressure
- customto separate the solvent
出典と根拠
- ORDレコード
- ord-5c1fdac029a140588c1ba6d6fc5c9073
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05417885
関連ノート
読み込み中…