反応式
[CH2:1]([O:8][C@H:9]1[C@H:14]([O:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C@@H:13]([CH2:23][O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[O:12][CH:11]=[CH:10]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:32]([O-:35])(O)=O.[Na+].[OH:37]OS([O-])=O.[K+].C(Cl)Cl.[CH3:46][C:47](C)=O>O>[CH2:1]([O:8][C@H:9]1[C@H:14]([O:15][CH2:16][C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[C@@H:13]([CH2:23][O:24][CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[O:12][C@@H:11]([O:35][CH2:32][CH:46]=[CH2:47])[C@@H:10]1[OH:37])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
実験手順
3,4,6-tri-O-benzyl-D-glucal (7.2 g, 17.3 mmol) in CH2Cl2/acetone (2:1, 105 mL) and a saturated solution of NaHCO3 (100 mL) was added. The mixture was stirred vigorously while a solution of Oxone (21.2 g, 34.6 mmol) in water (150 mL) was added dropwise over 30 minutes. After 1.5 hours of vigorous stirring the layers were separated, and the aqueous layer was extracted with CH2Cl2 (2×150 mL). The organic solutions were combined, dried over MgSO4, filtered and concentrated. The residue was co-evaporated with toluene (3×10 mL), dissolved in allyl alcohol (25 mL) and stirred at room temperature overnight. The reaction mixture was purified on a silica gel column (80 g) using an ISCO automated chromatography system, eluting with a 0→60% gradient of ethyl acetate in heptane, to give allyl 3,4,6-tri-O-benzyl-β-D-glucopyranoside (4.2 g, 50%).
後処理
- additionwas added dropwise over 30 minutes
- customwere separated
- extractionthe aqueous layer was extracted with CH2Cl2 (2×150 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- dissolutiondissolved in allyl alcohol (25 mL)
- stirringstirred at room temperature overnight
- customThe reaction mixture was purified on a silica gel column (80 g)
- washeluting with a 0→60% gradient of ethyl acetate in heptane
出典と根拠
- ORDレコード
- ord-bba88a93227143cebe8f3aba0f22b6a6
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447133B2
関連ノート
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