Water → HCID 178455744、化合物
反応式
Br[C:2](Br)=[CH:3][C@H:4]1[CH2:9][CH2:8][C@H:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:6][CH2:5]1.C([Li])CCC.O>O1CCCC1.CCCCCC>[C:3]([C@H:4]1[CH2:9][CH2:8][C@H:7]([CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:6][CH2:5]1)#[CH:2]参加物
反応条件
- 温度
- -70 °C
実験手順
A solution of 35.9 g of trans-1-(2,2-dibromovinyl)-4-pentylcyclohexane in 300 ml of absolute tetrahydrofuran at -70° C. was placed under argon gasification and treated within 20 minutes with 222 ml of a 1.2M solution of butyl lithium in hexane. The mixture was subsequently stirred at -70° C. for a further 2 hours, then poured into 1.2 l of water and extracted three times with 400 ml of hexane each time. The organic phases were washed twice with 400 ml of water each time, dried over magnesium sulphate and concentrated. Crystallization of the residue (19.4 g) from 250 ml of methanol at -78° C. gave 10.0 g of trans-1-ethynyl-4-pentylcyclohexane which was a colourless liquid at room temperature. Crystallization of the mother liquor, concentrated to about 100 ml, at -78° C. gave a further 3.9 g of trans-1-ethynyl-4-pentylcyclohexane. The combined batches of product were crystallized again from 300 ml of methanol at -78° C. and subsequently distilled (110° C./0.3 Torr), there being obtained 10.43 g (55%) of trans-1-ethynyl-4-pentylcyclohexane (purity 99.4%) as a colourless liquid; Rf-value (hexane) 0.41.
後処理
- customat -70° C.
- extractionextracted three times with 400 ml of hexane each time
- washThe organic phases were washed twice with 400 ml of water each time
- dry with materialdried over magnesium sulphate
- concentrationconcentrated
- customCrystallization of the residue (19.4 g) from 250 ml of methanol at -78° C.
出典と根拠
- ORDレコード
- ord-575348bfd5ec46fcbed5f023fe4c18d7
- 出典データセット
- uspto-grants-1986_06
- 特許番号
- US04595521
反応ノート
読み込み中…