反応式
[CH2:1]([SH:7])[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.[CH3:8][C:9](=[O:13])[CH:10]=[CH:11][CH3:12]>C(O)C>[O:6]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:1][S:7][CH:11]([CH3:12])[CH2:10][C:9](=[O:13])[CH3:8]参加物
4
実験手順
10 g of furfurylmercaptan and 15 g of 3-penten-2-one were dissolved in 100 ml of ethanol. The solution was stirred at room temperature for 48 hours. The solvent was then distilled off in vacuo at 50° C. The residue (18 g) was purified by preparative high pressure liquid chromatography (HPLC). 9 g of 4-[(furylmethyl)thio]-2-pentanone (purity 95%) were obtained. The IR, NMR and mass spectra of the compound agree with the structure described for it.
後処理
- distillationThe solvent was then distilled off in vacuo at 50° C
- customThe residue (18 g) was purified by preparative high pressure liquid chromatography (HPLC)
出典と根拠
- ORDレコード
- ord-d0b47cf1bf99457397c9e061e28d2c95
- 出典データセット
- uspto-grants-2000_11
- 特許番号
- US06153770
関連ノート
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