thiirane (E)-ethyl 7-(thiiran-2-yl)hept-6-enoate → Ethyl 5-(2,5-dihydrothiophen-2-yl)pentanoate
反応式
[CH2:1]([O:3][C:4](=[O:14])[CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]/[CH:11]1[CH2:13][S:12]1)[CH3:2].S1CC1>C1C=CC=CC=1>[S:12]1[CH2:13][CH:11]=[CH:10][CH:9]1[CH2:8][CH2:7][CH2:6][CH2:5][C:4]([O:3][CH2:1][CH3:2])=[O:14]参加物
3
実験手順
A solution of thiirane (E)-ethyl 7-(thiiran-2-yl)hept-6-enoate (40 mg, 0.19 mmol) and Cu(hfacac)2 (4.7 mg, 10 μmol) in benzene (20 mL) was heated at 120° C. for 1.5 h in a pressure tube. Concentration of the solvent in vacuo afforded a residue, which was purified by column chromatography (n-pentane) to give Ethyl 5-(2,5-dihydrothiophen-2-yl)pentanoate (32 mg, 80%) as a colorless oil.
後処理
- customConcentration of the solvent in vacuo afforded a residue, which
- customwas purified by column chromatography (n-pentane)
出典と根拠
- ORDレコード
- ord-389dec8c884e495fa9090ffecdf6d2af
- 出典データセット
- uspto-grants-2013_03
- 特許番号
- US08404872B2
反応ノート
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