Water → 1-Hexylcycloprop-1-ene
反応式
Br[C:2]1(Br)[CH2:4][C:3]1(Br)[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].C[Li].O>C(OCC)C>[CH2:5]([C:3]1[CH2:4][CH:2]=1)[CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]参加物
5
実験手順
A solution of 1.01 g (0.00278 mol) of 1,1,2-tribromo-2-hexyl-cyclopropane in 4 ml of diethyl ether was placed under a nitrogen atmosphere via use of a Firestone valve. While cooling in an ice water bath, 6.3 ml (0.00835 mol) of 1.4M methyl lithium in diethyl ether was added slowly by syringe. After 15 minutes, 2 ml of water was added via syringe. The resulting mixture was transferred to a separatory funnel and the phases were separated. The organic layer was dried over MgSO4 and filtered. The solvent was removed from the filtrate in vacuo with a bath temperature under 20° C. to yield 0.300 g (87% of theoretical) of 1-hexyl-cyclopropene pure as an oil.
後処理
- temperatureWhile cooling in an ice water bath
- customThe resulting mixture was transferred to a separatory funnel
- customthe phases were separated
- dry with materialThe organic layer was dried over MgSO4
- filtrationfiltered
- customThe solvent was removed from the filtrate in vacuo with a bath temperature under 20° C.
出典と根拠
- ORDレコード
- ord-26c0b651f1384c988b24009e56c91f96
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06365549B2
反応ノート
読み込み中…