反応式
[CH3:1][O:2][CH3:3].[CH2:4]([Li])CCC.[B:9]([O:14]C)([O:12]C)OC.[CH3:16][C:17]([OH:19])=O.[CH2:20]1[CH2:24][O:23][CH2:22][CH2:21]1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:16][C:17]2[O:19][CH2:20][CH2:24][O:23][C:22]=2[C:21]=1[B:9]([OH:12])[OH:14]参加物
6
実験手順
To a solution of methyl ether X (10.0 g, 60 mmol) in 50 ml THF at −78° C. was added n-butyllithium (36 ml, 90 mmol, 2.5 M in hexanes) was added drop-wise. After 1 h the solution was warmed to rt. After 1 h the solution was cooled to −78° C. and trimethyl borate (13.6 ml, 120 mmol) was added. The solution was warmed to rt. After 16 h the mixture was quenched by the addition of water and resulting mixture was acidified with AcOH and extracted with ethyl acetate. The combined organics were washed with saturated NaHCO3, dried with MgSO4, filtered and concentrated in vacuo. The resulting oil was azeotroped with toluene to afford 6-methoxy-2,3-dihydro-benzo[1,4]dioxin-5-yl-boronic acid (13.72 g, 98%) as an oil.
後処理
- additionwas added drop-wise
- temperatureAfter 1 h the solution was cooled to −78° C.
- temperatureThe solution was warmed to rt
- customAfter 16 h the mixture was quenched by the addition of water
- customresulting mixture
- extractionextracted with ethyl acetate
- washThe combined organics were washed with saturated NaHCO3
- dry with materialdried with MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe resulting oil was azeotroped with toluene
出典と根拠
- ORDレコード
- ord-a7fd0cf738bd462887f493f5d5fdd0f1
- 出典データセット
- uspto-grants-2010_12
- 特許番号
- US07858632B2
関連ノート
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