Ethanol → Ethyl 5-benzyloxypentanoate
反応式
[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([OH:15])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:16](O)[CH3:17].S(=O)(=O)(O)O>C(N(CC)CC)C>[CH2:1]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
5
実験手順
A mixture of 61.1 g of 5-benzyloxypentanoic acid, 566 ml of ethanol and 10 ml of concentrated sulfuric acid is refluxed for 15 h. The mixture is cooled to room temperature, 10 ml of triethylamine are added and evaporated. The residue is diluted with 250 ml of ether and the solution is washed in water and brine dried (MgSO4) and evaporated. The residual oil is distilled to give ethyl 5-benzyloxypentanoate, b.p. 110°-113° C. (0.7 mm/Hg).
後処理
- temperatureis refluxed for 15 h
- customevaporated
- additionThe residue is diluted with 250 ml of ether
- washthe solution is washed in water
- dry with materialbrine dried (MgSO4)
- customevaporated
- distillationThe residual oil is distilled
出典と根拠
- ORDレコード
- ord-6690fe47460a4ce08d4c3bc3fbdb9b2d
- 出典データセット
- uspto-grants-1994_12
- 特許番号
- US05371096
反応ノート
読み込み中…