反応式
[CH:1]#[C:2][CH2:3][CH2:4][CH2:5][CH2:6][C:7]#[CH:8].[Li]CCCC.C=[O:15].Cl.C1C[O:20][CH2:19][CH2:18]1>CCOCC>[CH2:1]([OH:15])[C:2]#[C:3][CH2:4][CH2:5][CH2:6][CH2:7][C:8]#[C:18][CH2:19][OH:20]参加物
7
反応条件
- 温度
- -78 °C
実験手順
2.12 g of commercially available 1,7 octadiyne (20.0 mmol) was first combined with 80 mL of Et2O and 30 mL of THF. The solution was cooled to -78° C. and treated with 15.6 mL (42 mmol, 2.7M) of BuLi. After 0.5 hr at this temperature, 4.8 g of paraformaldehyde (160 mmol) was added and stirred for a further 2.0 hr at 0° C. At 10% soln. of aqueous HCl was added and the crude product extracted into diethyl ether. Treatment of the ether extracts with sat. NaHCO3 and brine, followed by solvent removal and column chromatography (60:40 EtOAc: Hexane) gave pure deca-2,8-diyne-1,10-diol in 50% yield.
後処理
- extractionthe crude product extracted into diethyl ether
- customfollowed by solvent removal and column chromatography (60:40 EtOAc: Hexane)
出典と根拠
- ORDレコード
- ord-b19e511fb21e461cbc8699424a744fa4
- 出典データセット
- uspto-grants-1995_07
- 特許番号
- US05436361
関連ノート
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