反応式
[CH3:1][C:2]1CC[CH2:5][C:4]([CH3:9])([CH3:8])[C:3]=1/[CH:10]=[CH:11]/[C:12](/[CH3:40])=[CH:13]/[CH:14]=[CH:15]/[C:16](/[CH3:39])=[CH:17]/[CH:18]=[CH:19]/[CH:20]=[C:21](\[CH3:38])/[CH:22]=[CH:23]/[CH:24]=[C:25](\[CH3:37])/[CH:26]=[CH:27]/[C:28]1[C:33]([CH3:35])([CH3:34])[CH2:32][CH2:31][CH2:30][C:29]=1[CH3:36].C(Cl)(Cl)Cl.[OH2:45].[CH2:46]([OH:48])[CH3:47]>>[CH3:1][C:2]1[C:46](=[O:48])[CH2:47][CH2:5][C:4]([CH3:9])([CH3:8])[C:3]=1/[CH:10]=[CH:11]/[C:12](/[CH3:40])=[CH:13]/[CH:14]=[CH:15]/[C:16](/[CH3:39])=[CH:17]/[CH:18]=[CH:19]/[CH:20]=[C:21](\[CH3:38])/[CH:22]=[CH:23]/[CH:24]=[C:25](\[CH3:37])/[CH:26]=[CH:27]/[C:28]1[C:33]([CH3:35])([CH3:34])[CH2:32][CH2:31][C:30](=[O:45])[C:29]=1[CH3:36]参加物
5
実験手順
Into a flask was charged 0.5 gm of β-carotene and 10 ml of chloroform. The mixture is stirred to form a solution. Into this solution was charged 1.6 ml of the oxidant solution described in example 1. The mixture was stirred for 1.5 hours to complete the reaction. The phases were separated and the organic phase was washed with water once and evaporated to yield a residue that was dissolved in 10 ml of warm ethanol. This ethanol solution was added slowly to 50 ml of water to form a precipitate which was filtered and dried to yield 85% yield of canthaxanthin of approximately 80% purity.
後処理
- customto form a solution
- stirringThe mixture was stirred for 1.5 hours
- customthe reaction
- customThe phases were separated
- washthe organic phase was washed with water once
- customevaporated
- customto yield a residue that
- customto form a precipitate which
- filtrationwas filtered
- customdried
出典と根拠
- ORDレコード
- ord-bbaa20909ddd4b8a880e98272433b08a
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06372946B1
関連ノート
読み込み中…