Methyl chloroformate → Methyl hept-6-en-2-ynoate
反応式
[CH2:1]([Mg]Br)[CH:2]=[CH2:3].[CH2:6](Cl)[C:7]#[CH:8].Cl[C:11]([O:13][CH3:14])=[O:12]>CCOCC>[C:11]([O:13][CH3:14])(=[O:12])[C:3]#[C:2][CH2:1][CH2:8][CH:7]=[CH2:6]参加物
5
実験手順
A solution of allylmagnesium bromide (1M, 150 mL, 150 mmol) in ether under a nitrogen atmosphere was cooled to −10° C., and propargyl chloride (5.4 mL, 75 mmol) was added dropwise. The solution was stirred for 24 h at room temperature, and then cooled to 0° C. Methyl chloroformate was added dropwise, and the solution was allowed to stir at room temperature for 4 h. The reaction was quenched by cautious addition of satd aq NH4Cl (100 mL) at 0° C. The organic layer was washed with brine, dried, and evaporated to a residue. Chromatography on silica gel provided the title compound (4.5 g, 44%) as a pale yellow liquid.
後処理
- temperaturecooled to 0° C
- stirringto stir at room temperature for 4 h
- customThe reaction was quenched by cautious addition of satd aq NH4Cl (100 mL) at 0° C
- washThe organic layer was washed with brine
- customdried
- customevaporated to a residue
出典と根拠
- ORDレコード
- ord-2beb62d89a934b15a71321753b2ccb5b
- 出典データセット
- uspto-grants-2010_02
- 特許番号
- US07666861B2
反応ノート
読み込み中…