反応式
[NH:1]1[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]1.[CH2:7]([O:14][C:15](Cl)=[O:16])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.O>C(Cl)(Cl)Cl.C(N(CC)CC)C>[CH2:7]([O:14][C:15]([N:1]1[CH2:5][CH2:4][CH:3]([OH:6])[CH2:2]1)=[O:16])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1参加物
6
実験手順
30 g of 3-pyrrolidinol was dissolved in 500 ml of chloroform, to which 53 ml of triethylamine was added, followed by gradually dropping 52 ml of benzyloxycarbonyl chloride at room temperature. After completion of the reaction, the reaction solution was poured into water and extracted with chloroform. The solvent was distilled off under reduced pressure and the resultant residue was purified by column chromatography (eluting solvent: hexane-ethyl acetate) to obtain 70.67 g of the intended compound.
後処理
- additionwas added
- customat room temperature
- customAfter completion of the reaction
- extractionextracted with chloroform
- distillationThe solvent was distilled off under reduced pressure
- customthe resultant residue was purified by column chromatography (eluting solvent: hexane-ethyl acetate)
出典と根拠
- ORDレコード
- ord-5af16964b867449580fcd93f36e2a778
- 出典データセット
- uspto-grants-1995_11
- 特許番号
- US05468740
関連ノート
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