反応式
[CH:1]([CH:3]1[CH2:8][O:7][C:5](=[O:6])[CH2:4]1)=[CH2:2].C([O-])(=O)C.[Na+].[CH3:14][OH:15]>>[OH:15][CH2:14][CH:3]([CH:1]=[CH2:2])[CH2:4][C:5]([O:7][CH3:8])=[O:6]参加物
4
実験手順
A solution of RS 3-vinylbutyrolactone (3.5 g) and sodium acetate (2.56 g) in methanol (30 ml) was kept for 20 hours. Solvent was evaporated and the residue was partitioned between water and ether. The aqueous layer was extracted twice more with ether and the extracts combined, filtered through phase separating paper and evaporated. The residue was purified by filtration chromatography on silica gel (Merck 7736) starting with 1/9 ethyl acetate/hexane and progressing to 4/6 ethyl acetate/hexane as eluent to give methyl 4-hydroxy-3-vinylbutyrate as an oil; NMR(CDCl3) δ5.73(1H,m), 5.15(2H,m), 3.68(3H,s), 3.60(2H,t), 2.76(1H,m), 2.48(2H,m), 1.69(1H,t); m/e 145(M+H)+.
後処理
- customSolvent was evaporated
- customthe residue was partitioned between water and ether
- extractionThe aqueous layer was extracted twice more with ether
- filtrationfiltered through phase
- customseparating paper
- customevaporated
- filtrationThe residue was purified by filtration chromatography on silica gel (Merck 7736)
出典と根拠
- ORDレコード
- ord-70448c2a831c44479f92ea6ac8088e19
- 出典データセット
- uspto-grants-1996_09
- 特許番号
- US05556977
関連ノート
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