反応式
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.C([Li])CCC.C([O:18][B:19](OCCCC)[O:20]CCCC)CCC>C(OCC)C>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([B:19]([OH:20])[OH:18])=[CH:3][CH:4]=1参加物
5
反応条件
- 温度
- 0 °C
実験手順
To a solution of 4-iodotoluene (35 g, 160.5 mmol) in diethyl ether (400 mL) was added n-butyllithium (2 M in pentane, 88.3 mL, 176.6 mmol) at 0° C. After stirring at 0° C. for another 15 min the solution was cooled to −60° C. and tributylborate (60.6 mL, 224.7 mmol) was added. The cooling bath was removed and the reaction allowed to heat up to room temperature. The solution was acidified with hydrochloric acid (2 N, 280 mL) and the organic phase separated off. The aqueous phase was extracted with diethyl ether 2×125 mL). The combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL). The combined aqueous extracts were acidified to give 18.6 g of the desired material.
後処理
- temperaturewas cooled to −60° C.
- customThe cooling bath was removed
- temperatureto heat up to room temperature
- customthe organic phase separated off
- extractionThe aqueous phase was extracted with diethyl ether 2×125 mL)
- extractionThe combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL)
出典と根拠
- ORDレコード
- ord-74803c53f6274e458b772a5e05af20cd
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06706749B2
関連ノート
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