反応式
[CH3:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[C:3]=1/[CH:10]=[CH:11]/[C:12](/[CH3:21])=[CH:13]/[CH:14]=[CH:15]/[C:16](/[CH3:20])=[CH:17]/[CH:18]=O.Cl>O1CCCC1>[CH3:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[C:3]=1/[CH:10]=[CH:11]/[C:12](/[CH3:21])=[CH:13]/[CH:14]=[CH:15]/[C:16](/[CH3:20])=[CH:17]/[CH:18]=[CH:18]/[CH:17]=[C:16](\[CH3:20])/[CH:15]=[CH:14]/[CH:13]=[C:12](\[CH3:21])/[CH:11]=[CH:10]/[C:3]1[C:4]([CH3:9])([CH3:8])[CH2:5][CH2:6][CH2:7][C:2]=1[CH3:1]参加物
実験手順
A slurry of titanium trichloride (770 mg, 5.0 mmol) in 20 ml dry tetrahydrofuran was prepared under an inert atmosphere (nitrogen or argon), and magnesium turnings (120 mg, 5.0 mmol) were added. The resulting mixture was refluxed overnight to form the Ti(II) reagent, and a solution of retinal (710 mg, 2.5 mmol) in 5 ml dry tetrahydrofuran was added. After refluxing for two hours, the solution was poured into 50 ml 2 N aqueous hydrochloric acid and extracted several times with ether. The ether extracts were combined, washed with saturated aqueous sodium chloride solution, dried sulfate, and concentrated by solvent removal at the rotary evaporator. The residue was purified by chromatography over silica gel. Elution with hexane gave 130 mg (20% yield) beta-carotene identified by thin-layer chromatographic comparison with an authentic sample, and by its characteristic ultraviolet spectrum.
後処理
- temperatureAfter refluxing for two hours
- extractionextracted several times with ether
- washwashed with saturated aqueous sodium chloride solution, dried sulfate
- concentrationconcentrated by solvent removal at the rotary evaporator
- customThe residue was purified by chromatography over silica gel
- washElution with hexane
出典と根拠
- ORDレコード
- ord-2ca4736e40054782a50c85c5dc13f772
- 出典データセット
- uspto-grants-1980_09
- 特許番号
- US04225734
関連ノート
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