反応式
[CH:1]1[CH2:5][CH:4]=[CH:3][CH:2]=1.[C:6]([O:10][CH3:11])(=[O:9])C=C.[CH3:12][CH2:13]OCC>>[CH:2]12[CH2:1][CH:5]([CH:12]=[CH:13]1)[CH2:4][CH:3]2[C:6]([O:10][CH3:11])=[O:9]参加物
4
実験手順
In 100 ml of anhydrous ether at 0° C. is mixed 30 ml of cyclopentadiene and 32 ml of methyl acrylate. The ice bath is removed and the mixture allowed to stir overnight. The solvent, unreacted methyl acrylate, and cyclopentadiene are removed at ambient temperature at reduced pressure; as less material distilled out of the mixture the pressure is gradually reduced to 0.5 mm. The desired epimeric mixture of methyl carboxylates is distilled at 42°-43° and 0.5 mm; ir: 3118, 3060, 2965, 2941, 2862, 1734, 1428, 1329, 1264, 1190, 1024, 704, cm-1 ; 60 MHz NMR: endo/exo=80/20.
後処理
- customThe ice bath is removed
- customThe solvent, unreacted methyl acrylate, and cyclopentadiene are removed at ambient temperature at reduced pressure
- distillationas less material distilled out of the mixture the pressure
- additionThe desired epimeric mixture of methyl carboxylates
- distillationis distilled at 42°-43°
出典と根拠
- ORDレコード
- ord-aea44e4176e348358cf8d2cd257d865a
- 出典データセット
- uspto-grants-1998_01
- 特許番号
- USRE035717
関連ノート
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